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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 10-Q

(Mark One)

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the Quarterly Period Ended September 30, 2023

OR

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from                      to

Commission File Number: 001-39450

HARMONY BIOSCIENCES HOLDINGS, INC.

(Exact name of registrant as specified in its charter)

Delaware

82-2279923

(State or other jurisdiction of
incorporation or organization)

(I.R.S. Employer
Identification No.)

630 W. Germantown Pike, Suite 215, Plymouth Meeting, PA

19462

(Address of principal executive offices)

(Zip Code)

(484) 539-9800

(Registrant’s telephone number, including area code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

    

Trading
Symbol(s)

    

Name of each exchange
on which registered

Common Stock, par value $0.00001 value per share

 

HRMY

 

The Nasdaq Stock Market LLC
(Nasdaq Global Market)

Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.   Yes      No   

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).   Yes    No  

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act:

Large accelerated filer

Accelerated filer

Non-accelerated filer

Smaller reporting company

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).   Yes     No  

As of October 27, 2023, there were 58,571,944 shares of the registrant’s common stock, par value $0.00001 value per share, outstanding.

TABLE OF CONTENTS

Page

Part I. Financial Information

3

Item 1. Financial Statements

3

Condensed Consolidated Balance Sheets (Unaudited)

3

Condensed Consolidated Statements of Operations and Comprehensive Income (Unaudited)

4

Condensed Consolidated Statements of Stockholders’ Equity (Unaudited)

5

Condensed Consolidated Statements of Cash Flows (Unaudited)

6

Notes to Condensed Consolidated Financial Statements (Unaudited)

7

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

23

Item 3. Quantitative and Qualitative Disclosures About Market Risk

36

Item 4. Controls and Procedures

37

Part II. Other Information

37

Item 1. Legal Proceedings

37

Item 1A. Risk Factors

38

Item 2. Unregistered Sales of Equity Securities, Use of Proceeds, and Issuer Purchases of Equity Securities

38

Item 3. Defaults upon Senior Securities

38

Item 4. Mine Safety Disclosures

39

Item 5. Other Information

39

Item 6. Exhibits

39

Signatures

40

2

PART I. FINANCIAL INFORMATION

Item 1. Financial Statements

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARY

UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS

(In thousands, except share and per share data)

    

September 30, 

    

December 31, 

    

2023

    

2022

ASSETS

 

  

 

  

CURRENT ASSETS:

 

  

 

  

Cash and cash equivalents

$

324,603

$

243,784

Investments, short-term

46,071

79,331

Trade receivables, net

 

67,264

 

54,740

Inventory, net

 

5,087

 

4,297

Prepaid expenses

 

14,269

 

9,347

Other current assets

 

5,704

 

8,786

Total current assets

 

462,998

 

400,285

NONCURRENT ASSETS:

 

  

 

  

Property and equipment, net

 

428

 

573

Restricted cash

 

250

 

750

Investments, long-term

67,700

22,568

Intangible assets, net

 

143,069

 

160,953

Deferred tax asset

100,485

85,943

Other noncurrent assets

 

2,836

 

2,798

Total noncurrent assets

 

314,768

 

273,585

TOTAL ASSETS

$

777,766

$

673,870

LIABILITIES AND STOCKHOLDERS’ EQUITY

 

  

 

  

CURRENT LIABILITIES:

 

  

 

  

Trade payables

$

6,539

$

3,786

Accrued compensation

 

10,322

 

11,532

Accrued expenses

 

72,761

 

59,942

Current portion of long-term debt

15,000

2,000

Other current liabilities

 

7,786

 

1,624

Total current liabilities

 

112,408

 

78,884

NONCURRENT LIABILITIES:

 

  

 

  

Long-term debt, net

 

182,131

 

189,647

Other noncurrent liabilities

 

1,895

 

2,501

Total noncurrent liabilities

 

184,026

 

192,148

TOTAL LIABILITIES

 

296,434

 

271,032

COMMITMENTS AND CONTINGENCIES (Note 12)

 

  

 

  

STOCKHOLDERS’ EQUITY:

 

  

 

  

Common stock—$0.00001 par value; 500,000,000 shares authorized at September 30, 2023 and December 31, 2022, respectively; 58,571,944 shares and 59,615,731 issued and outstanding at September 30, 2023 and December 31, 2022, respectively

 

1

 

1

Additional paid in capital

 

651,731

 

675,118

Accumulated other comprehensive (loss) income

(516)

(151)

Accumulated deficit

 

(169,884)

 

(272,130)

TOTAL STOCKHOLDERS’ EQUITY

 

481,332

 

402,838

TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY

$

777,766

$

673,870

The accompanying notes are an integral part of the unaudited condensed consolidated financial statements

3

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARY

UNAUDITED CONDENSED CONSOLIDATED

STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME

(In thousands, except share and per share data)

Three Months Ended September 30, 

Nine Months Ended September 30, 

    

2023

    

2022

    

2023

    

2022

Net product revenues

$

160,268

$

117,206

$

413,610

$

309,547

Cost of product sold

 

32,296

 

22,959

 

78,084

 

56,596

Gross profit

 

127,972

 

94,247

 

335,526

 

252,951

Operating expenses:

 

  

 

  

 

  

 

  

Research and development

 

17,499

 

40,548

 

45,757

 

60,794

Sales and marketing

 

23,418

 

20,467

 

70,518

 

58,210

General and administrative

 

22,546

 

21,331

 

67,417

 

61,374

Total operating expenses

 

63,463

 

82,346

 

183,692

 

180,378

Operating income

 

64,509

 

11,901

 

151,834

 

72,573

Loss on debt extinguishment

 

(9,766)

 

 

(9,766)

 

Other (expense) income, net

 

(5)

 

56

 

(34)

 

96

Interest expense, net

 

(2,906)

 

(3,990)

 

(8,327)

 

(12,086)

Income before income taxes

 

51,832

 

7,967

 

133,707

 

60,583

Income tax (expense) benefit

 

(13,371)

 

79,976

 

(31,461)

 

72,376

Net income

$

38,461

$

87,943

$

102,246

$

132,959

Unrealized income (loss) on investments

 

6

 

(149)

 

(365)

 

(178)

Comprehensive income

$

38,467

$

87,794

$

101,881

$

132,781

EARNINGS PER SHARE:

 

  

 

  

 

  

 

  

Basic

$

0.64

$

1.48

$

1.71

$

2.25

Diluted

$

0.63

$

1.44

$

1.68

$

2.18

Weighted average number of shares of common stock - basic

 

59,863,102

 

59,234,720

 

59,856,941

 

59,070,063

Weighted average number of shares of common stock - diluted

 

60,681,676

 

61,207,625

 

60,892,992

 

60,921,482

The accompanying notes are an integral part of the unaudited condensed consolidated financial statements

4

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARY

UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

(In thousands, except share and per share data)

Accumulated

Additional

other

Total

Common Stock

paid-in

comprehensive

Accumulated

stockholders’

   

Shares

   

Amount

   

capital

   

(loss) income

   

deficit

   

equity

Balance as of December 31, 2022

 

59,615,731

$

1

$

675,118

$

(151)

$

(272,130)

$

402,838

Net income

 

 

 

 

102,246

 

102,246

Unrealized loss on investments

(365)

(365)

Repurchase of common stock

(1,439,792)

(50,543)

(50,543)

Exercise of options and restricted stock units

 

396,005

 

 

4,314

 

 

4,314

Stock-based compensation

 

 

 

22,842

 

 

22,842

Balance as of September 30, 2023

 

58,571,944

$

1

$

651,731

$

(516)

$

(169,884)

$

481,332

Accumulated

Additional

other

Total

Common Stock

paid-in

comprehensive

Accumulated

stockholders’

   

Shares

   

Amount

   

capital

   

(loss) income

   

deficit

   

equity

Balance as of June 30, 2023

59,999,658

$

1

$

694,038

$

(522)

$

(208,345)

$

485,172

Net income

 

 

 

 

38,461

 

38,461

Unrealized loss on investments

6

6

Repurchase of common stock

(1,439,792)

(50,543)

(50,543)

Exercise of options

 

12,078

 

 

245

 

 

245

Stock-based compensation

 

 

 

7,991

 

 

7,991

Balance as of September 30, 2023

 

58,571,944

$

1

$

651,731

$

(516)

$

(169,884)

$

481,332

    

    

  

    

  

Accumulated

    

  

    

  

Additional

other

Total

Common Stock

paid-in

comprehensive

Accumulated

stockholders’

    

Shares

    

Amount

    

capital

(loss) income

    

deficit

    

equity

Balance as of December 31, 2021

 

58,825,769

$

1

$

640,104

$

$

(453,598)

$

186,507

Net income

 

 

 

 

132,959

 

132,959

Unrealized loss on investments

(178)

(178)

Issuance of common stock

8,050

408

408

Exercise of stock options

 

470,589

 

 

5,275

 

 

5,275

Stock-based compensation

 

 

 

18,913

 

 

18,913

Balance as of September 30, 2022

 

59,304,408

$

1

$

664,700

$

(178)

$

(320,639)

$

343,884

    

    

  

    

  

Accumulated

    

  

    

  

Additional

other

Total

Common Stock

paid-in

comprehensive

Accumulated

stockholders’

    

Shares

    

Amount

    

capital

(loss) income

    

deficit

    

equity

Balance as of June 30, 2022

 

59,117,749

$

1

$

655,143

$

(29)

$

(408,582)

$

246,533

Net income

 

 

 

 

87,943

 

87,943

Unrealized loss on investments

(149)

(149)

Issuance of common stock

8,050

408

408

Exercise of options

 

178,609

 

 

2,143

 

 

2,143

Stock-based compensation

 

 

 

7,006

 

 

7,006

Balance as of September 30, 2022

 

59,304,408

$

1

$

664,700

$

(178)

$

(320,639)

$

343,884

The accompanying notes are an integral part of the unaudited condensed consolidated financial statements

5

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARY

UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands, except share and per share data)

    

Nine Months Ended September 30, 

    

2023

    

2022

CASH FLOWS FROM OPERATING ACTIVITIES

 

  

 

  

Net income

$

102,246

$

132,959

Adjustments to reconcile net income to net cash used in operating activities:

 

 

  

Depreciation

 

350

 

312

Intangible amortization

 

17,884

 

17,005

Stock-based and employee stock purchase compensation expense

 

22,842

 

18,913

Stock appreciation rights market adjustment

 

(531)

 

321

Debt issuance costs amortization

 

2,089

 

1,241

Deferred taxes

(14,542)

(81,679)

Amortization of premiums and accretion of discounts on Investment securities

(2,031)

Loss on debt extinguishment

9,766

Other non-cash expenses

1,258

1,042

Change in operating assets and liabilities:

 

 

  

Trade receivables

 

(12,524)

 

(20,222)

Inventory

 

(790)

 

532

Prepaid expenses and other assets

 

(1,759)

 

(4,704)

Trade payables

 

2,753

 

9,048

Accrued expenses and other current liabilities

 

15,714

 

43,171

Other non-current liabilities

 

(3)

 

(151)

Net cash provided by operating activities

 

142,722

 

117,788

CASH FLOWS FROM INVESTING ACTIVITIES:

 

  

 

  

Purchase of investment securities

(105,856)

(55,637)

Proceeds from maturities and sales of investment securities

95,687

872

Purchase of property and equipment

 

(205)

 

(172)

Milestone payments

 

 

(40,000)

Net cash used in investing activities

 

(10,374)

 

(94,937)

CASH FLOWS FROM FINANCING ACTIVITIES:

 

  

 

  

Proceeds from issuance of common stock

408

Proceeds from long term debt

 

200,000

 

Debt issuance costs

 

(2,997)

 

Extinguishment of debt

 

(196,500)

 

Extinguishment of debt exit fees

 

(5,846)

 

Principal repayment of long term debt

(1,000)

(1,500)

Repurchase of common stock

(50,000)

Payments of employee withholding taxes related to stock-based awards

(514)

Proceeds from exercised options

 

4,828

 

5,275

Net cash (used in) provided by financing activities

 

(52,029)

 

4,183

NET INCREASE IN CASH, CASH EQUIVALENTS, AND RESTRICTED CASH

 

80,319

 

27,034

CASH, CASH EQUIVALENTS, AND RESTRICTED CASH—Beginning of period

 

244,534

 

235,059

CASH, CASH EQUIVALENTS, AND RESTRICTED CASH—End of period

$

324,853

$

262,093

Supplemental Disclosure of Cash Flow Information:

 

  

 

  

Cash paid during the year for interest

$

15,653

$

11,334

Cash paid during the year for taxes

36,543

9,702

The accompanying notes are an integral part of the unaudited condensed consolidated financial statements

6

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARY

NOTES TO UNAUDITED CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

(In thousands, except share and per share data)

1. ORGANIZATION AND DESCRIPTION OF BUSINESS

The Company

Harmony Biosciences Holdings, Inc., and its consolidated subsidiary (the “Company”) was founded in July 2017 as Harmony Biosciences II, LLC, a Delaware limited liability company. The Company converted to a Delaware corporation named Harmony Biosciences II, Inc. in September 2017 and, in February 2020, the Company changed its name to Harmony Biosciences Holdings, Inc. The Company’s operations are conducted in its wholly owned subsidiary, Harmony Biosciences, LLC (“Harmony”), which was formed in May 2017. The Company is a commercial-stage pharmaceutical company focused on developing and commercializing innovative therapies for patients living with rare neurological diseases as well as patients living with other neurological diseases who have unmet medical needs. The Company is headquartered in Plymouth Meeting, Pennsylvania.

2. LIQUIDITY AND CAPITAL RESOURCES

The unaudited condensed consolidated financial statements have been prepared as though the Company will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business. The Company had an accumulated deficit of $169,884 and $272,130, as of September 30, 2023 and December 31, 2022, respectively. As of September 30, 2023, the Company had cash, cash equivalents and investments of $438,374.

The Company believes that its existing cash, cash equivalents and investments on hand as of September 30, 2023, as well as additional cash generated from operating and financing activities will meet its operational liquidity needs and fund its planned investing activities for the next twelve months from the date of issuance of these unaudited condensed consolidated financial statements.

3. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of Presentation

The unaudited condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”) and include all adjustments necessary for the fair presentation of the Company’s financial position for the periods presented. All intercompany accounts and transactions have been eliminated in consolidation. The unaudited condensed consolidated balance sheet as of September 30, 2023, the unaudited condensed consolidated statements of cash flows for the three and nine months ended September 30, 2023, and 2022, and the unaudited condensed consolidated statements of operations and comprehensive income and the unaudited condensed consolidated statements of shareholders’ equity for the three and nine months ended September 30, 2023 and 2022, are unaudited. The balance sheet as of December 31, 2022, was derived from audited financial statements as of and for the year ended December 31, 2022. The unaudited interim condensed consolidated financial statements have been prepared on the same basis as the audited annual financial statements as of and for the year ended December 31, 2022, and, in the opinion of management, reflect all adjustments, which include only normal recurring adjustments, necessary for the fair presentation of the Company’s financial position as of September 30, 2023, and the results of its operations and its cash flows for the three and nine months ended September 30, 2023 and 2022. The unaudited condensed consolidated results of operations are not necessarily indicative of the results that may occur for the full fiscal year. Certain information and disclosures normally included in the financial statements prepared in accordance with GAAP have been condensed or omitted under the SEC’s rules and regulations. These unaudited condensed consolidated financial statements should be read

7

in conjunction with the audited financial statements and accompanying notes thereto contained in the Company’s Annual Report on Form 10-K for the year ended December 31, 2022.

Use of Estimates

The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts and disclosures in the unaudited condensed consolidated financial statements, including the notes thereto, and elsewhere in this report. Actual results may differ significantly from estimates, which include rebates due pursuant to commercial and government contracts, accrued research and development expenses, stock-based compensation expense and income taxes.

Cash, Cash Equivalents and Restricted Cash

Cash and cash equivalents and restricted cash consist of cash and, if applicable, highly liquid investments with an original maturity of three months or less when purchased, including investments in Money Market Funds and debt securities that approximate fair value. The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheet and the statements of cash flows.

    

As of

    

September 30, 

    

December 31, 

2023

2022

Cash and cash equivalents

$

324,603

$

243,784

Restricted cash

 

250

 

750

Total cash, cash equivalents, and restricted cash shown in the statements of cash flows

$

324,853

$

244,534

Restricted cash includes amounts required to be held as a security deposit in the form of letters of credit for the Company’s credit card program and the fleet program.

Investments

The Company’s investments consist of debt securities that are classified as available-for-sale. Short-term and long-term investments are carried at fair value and unrealized gains and losses are recorded as a component of accumulated comprehensive income in stockholders’ equity. The amortization of premiums and accretion of discounts adjust the carrying value of investments and are recorded in interest expense, net, on the unaudited condensed consolidated statements of operations and comprehensive income. Interest income and realized gains and losses, if any, are also recorded in interest expense, net, on the unaudited condensed consolidated statement of operations and comprehensive income. Realized gains and losses that result from the sale of investments are determined on a specific identification basis.

At each reporting period, the Company reviews any unrealized losses position to determine if the decline in the fair value of the underlying investments is a result of credit losses or other factors. If the assessment indicates that a credit loss exists, any impairment is recognized as an allowance for credit losses in our consolidated statement of operations.

Interest income generated from our investments and cash equivalents, which is included in interest expense, net, was $3,384 and $8,537 for the three and nine months ended September 30, 2023, respectively, compared to $828 and $1,145 for the three and nine months ended September 30, 2022, respectively.

Concentrations of Risk

Substantially all of the Company’s cash and money market funds are held in four financial institutions. Due to their size, the Company believes these financial institutions represent minimal credit risk. Deposits may

8

exceed the amount of insurance provided on such deposits by the Federal Deposit Insurance Corporation for U.S. institutions. The Company has not experienced any losses on its deposits of cash and cash equivalents. The Company believes that it is not exposed to significant credit risk due to the financial position of the depository institutions in which those deposits are held.

The Company is subject to credit risk from its trade receivables related to its product sales. The Company extends credit to specialty pharmaceutical distribution companies within the United States. Customer creditworthiness is monitored, and collateral is not required. Historically, the Company has not experienced credit losses on its accounts receivable. The Company monitors its exposure within accounts receivable and would record a reserve against uncollectible accounts receivable if necessary. As of September 30, 2023, three customers accounted for 100% of gross accounts receivable; Caremark LLC (“CVS Caremark”), which accounted for 37% of gross accounts receivable; Accredo Health Group, Inc. (“Accredo”), which accounted for 37% of gross accounts receivable; and PANTHERx Specialty Pharmacy LLC (“Pantherx”), which accounted for 26% of gross accounts receivable. As of December 31, 2022, three customers accounted for 100% of gross accounts receivable; CVS Caremark, which accounted for 41% of gross accounts receivable, Accredo, which accounted for 35% of gross accounts receivable; and Pantherx, which accounted for 24% of gross accounts receivable.

For the nine months ended September 30, 2023, three customers accounted for 100% of gross product revenues; CVS Caremark accounted for 37% of gross product revenues; Accredo accounted for 32% of gross product revenues; and Pantherx accounted for 31% of gross product revenues. For the nine months ended September 30, 2022, three customers accounted for 100% of gross product revenues; CVS Caremark accounted for 40% of gross product revenues; Pantherx accounted for 30% of gross product revenues; and Accredo accounted for 30% of gross product revenues.

The Company depends on a single source supplier for each of its product and active pharmaceutical ingredient.

Share Repurchases

The Company accounts for share repurchases as constructive retirements, whereby it reduces common stock and additional paid-in capital by the amount of the original issuance, with any excess purchase price recorded as a reduction to retained earnings. Under this method, issued and outstanding shares of common stock are reduced by the amount of shares of common stock repurchased, and no treasury stock is recognized on the condensed consolidated financial statements.

Recently Issued Accounting Pronouncements

The Company did not adopt any new accounting pronouncements that had a material effect on its condensed consolidated financial statements during the three and nine months ended September 30, 2023.

9

4. INVESTMENTS

The carrying value and amortized cost of the Company’s available-for-sale debt securities, summarized by type of security, consisted of the following:

September 30, 2023

Amortized

Unrealized

Unrealized

Fair

Cost

Gains

Losses

Value

Short-term:

Commercial paper

$

27,717

1

(13)

$

27,705

Corporate debt securities

16,456

3

(7)

16,452

U.S. government securities

1,915

(1)

1,914

Total short-term investments

$

46,088

4

(21)

$

46,071

Long-term:

Commercial paper

$

1,623

(2)

$

1,621

Corporate debt securities

39,497

14

(155)

39,356

U.S. government securities

27,079

(356)

26,723

Total long-term investments

$

68,199

14

(513)

$

67,700

December 31, 2022

Amortized

Unrealized

Unrealized

Fair

Cost

Gains

Losses

Value

Short-term:

Commercial paper

$

26,553

15

(34)

$

26,534

Corporate debt securities

49,213

9

(73)

49,149

U.S. government securities

3,658

(10)

3,648

Total short-term investments

$

79,424

24

(117)

$

79,331

Long-term:

Commercial paper

$

853

1

$

854

Corporate debt securities

21,516

11

(68)

21,459

U.S. government securities

257

(2)

255

Total long-term investments

$

22,626

12

(70)

$

22,568

The Company classifies investments with an original maturity of less than one year as current and investments with an original maturity date of greater than one year as noncurrent on its unaudited condensed consolidated balance sheet. The investments classified as noncurrent have original maturity dates ranging from 1-2 years. The Company did not have any available-for-sale debt security investments in a continuous unrealized loss position of greater than 12 months as of September 30, 2023 and December 31, 2022, respectively.

5. FAIR VALUE MEASUREMENTS

The Company’s unaudited condensed consolidated financial statements include cash, cash equivalents, restricted cash, accounts payable, and accrued liabilities, all of which are short term in nature and, accordingly, approximate fair value.

10

It is the Company’s policy to measure non-financial assets and liabilities at fair value on a nonrecurring basis. These non-financial assets and liabilities are not measured at fair value on an ongoing basis but are subject to fair value adjustments in certain circumstances (such as evidence of impairment), which, if material, are disclosed in the accompanying footnotes.

The Company measures certain assets and liabilities at fair value based on the fair value hierarchy that prioritizes inputs to valuation techniques used to measure fair value into three levels based on the source of inputs as follows:

Level 1—Valuations based on unadjusted quoted prices in active markets for identical assets or liabilities.

Level 2—Valuations based on observable inputs and quoted prices in active markets for similar assets and liabilities.

Level 3—Valuations based on unobservable inputs and models that are supported by little or no market activity.

Money market funds are classified as Level 1 fair value instruments. Investments in available-for-sale debt securities are classified as Level 2 and carried at fair value, which we estimate utilizing a third-party pricing service. The pricing service utilizes industry standard valuation models whereby all significant inputs, including benchmark yields, reported trades, broker/dealer quotes, issuer spreads, bids, offers, or other market-related data, are observable. We validate valuations obtained from third-party services by obtaining market values from other pricing sources. The Company did not classify any assets or liabilities as Level 3 as of September 30, 2023 or December 31, 2022.

The Company’s assets measured at fair value consisted of the following:

September 30, 2023

December 31, 2022

Total

Level 1

Level 2

Total

Level 1

Level 2

Assets

Cash equivalents

$

198,135

198,135

$

184,977

184,977

Commercial paper

29,326

29,326

27,388

27,388

Corporate debt securities

55,808

55,808

70,608

70,608

U.S. government securities

28,637

28,637

3,903

3,903

Total

$

311,906

198,135

113,771

$

286,876

184,977

101,899

6. INVENTORY

Inventory, net consisted of the following:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Raw materials

$

932

$

838

Work in process

 

1,833

 

1,513

Finished goods

 

2,611

 

2,565

Inventory, gross

 

5,376

 

4,916

Reserve for excess inventory

 

(289)

 

(619)

Total inventory, net

$

5,087

$

4,297

11

7. INTANGIBLE ASSETS

In August 2019, the Company received FDA approval of WAKIX® (pitolisant) for the treatment of excessive daytime sleepiness (“EDS”) in adult patients with narcolepsy. This event triggered a milestone payment of $75,000 under the provisions of the 2017 LCA (defined below) which the Company capitalized as an intangible asset. The Company determined a useful life of 10 years for such intangible asset, and, as of September 30, 2023, the remaining useful life was 6.0 years.

In October 2020, the Company received FDA approval for the New Drug Application (“NDA”) for WAKIX for the treatment of cataplexy in adult patients with narcolepsy. This event triggered a milestone payment of $100,000 under the provisions of the 2017 LCA which the Company capitalized as an intangible asset and paid in January of 2021. The Company determined a useful life of 9 years for such intangible asset, and, as of September 30, 2023, the remaining useful life was 6.0 years.

In February 2022, the Company attained $500,000 in life-to-date aggregate net sales of WAKIX in the United States. This event triggered a final $40,000 payment under the provisions of the 2017 LCA which the Company capitalized as an intangible asset and paid in March of 2022. The Company determined a useful life of 7.6 years for such intangible asset, and, as of September 30, 2023, the remaining useful life was 6.0 years.

Amortization expense was $5,962 and $5,961 for the three months ended September 30, 2023 and 2022, respectively, and $17,884 and $17,005 for the nine months ended September 30, 2023 and 2022, respectively, and is recorded in general and administrative expenses on the unaudited condensed consolidated statements of operations and comprehensive income.

The Company expects the future annual amortization expense for the unamortized intangible assets to be as follows:

Years ending December 31, 

    

2023 (Excluding the nine months ended September 30, 2023)

$

5,961

2024

 

23,845

2025

 

23,845

2026

 

23,845

2027

 

23,845

Thereafter

41,728

Total

$

143,069

The gross carrying amount and net book value of the intangible asset is as follows:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Gross Carrying Amount

$

215,000

$

215,000

Accumulated Amortization

 

(71,931)

 

(54,047)

Net Book Value

$

143,069

$

160,953

8. LICENSE AGREEMENTS AND ASSET PURCHASE AGREEMENTS

License Agreements

In July 2017, Harmony entered into a License Agreement (the “2017 LCA”) with Bioprojet Société Civile de Recherche (“Bioprojet”) whereby Harmony acquired the exclusive right to commercialize the pharmaceutical compound pitolisant for the treatment, and/or prevention, of narcolepsy, obstructive sleep apnea, idiopathic hypersomnia, and Parkinson’s disease as well as any other indications unanimously agreed by the parties in the United States and its territories. A milestone payment of $50,000 was due upon acceptance by the FDA of

12

pitolisant’s NDA, which was achieved in February 2019 and was expensed within research and development for the year ended December 31, 2019. A milestone payment of $77,000, which included a $2,000 fee that is described below, was due upon FDA approval of WAKIX (pitolisant) for treatment of EDS in adult patients with narcolepsy, which was achieved in August 2019. The $2,000 payment and $75,000 milestone payment were paid in August and November 2019, respectively. In addition, a milestone payment of $102,000, which included a $2,000 fee was due upon the FDA approval of the NDA for WAKIX for the treatment of cataplexy in adult patients with narcolepsy. The $2,000 payment was paid in October 2020 and a $100,000 milestone payment was paid in January 2021. A final $40,000 milestone payment was paid to Bioprojet in March 2022 upon WAKIX attaining $500,000 in aggregate net sales in the United States. The 2017 LCA also requires a fixed trademark royalty and a tiered royalty based on net sales, which is payable to Bioprojet on a quarterly basis. The Company incurred $29,665 and $20,944 for the three months ended September 30, 2023 and 2022, respectively, and $71,267 and $51,741 for the nine months ended September 30, 2023 and 2022, respectively, for sales-based, trademark and tiered royalties recognized as cost of product sold. As of September 30, 2023 and December 31, 2022, the Company had accrued $29,665 and $25,367, respectively, for sales-based, trademark and tiered royalties.  

On July 31, 2022, Harmony entered into a License and Commercialization Agreement (the “2022 LCA”) with Bioprojet whereby Harmony obtained exclusive rights to manufacture, use and commercialize one or more new products based on pitolisant in the United States and Latin America, with the potential to add additional indications and formulations upon agreement of both parties. Harmony paid an initial, non-refundable $30,000 licensing fee in October 2022 and additional payments of up to $155,000 are potentially due under the 2022 LCA upon the achievement of certain future development and sales-based milestones. In addition, there are other payments due upon achievement of development milestones for new indications and formulations as agreed upon by both parties. The 2022 LCA also requires a fixed trademark royalty and a tiered royalty based on net sales upon commercialization, which will be payable to Bioprojet on a quarterly basis.

Agreement Related to Intellectual Property

In August 2021, the Company entered into an asset purchase agreement with ConSynance Therapeutics, Inc. (the “APA”) to acquire HBS-102 (formerly referred to as “CSTI-100”), a potential first-in-class molecule with a novel mechanism of action. Under the terms of the APA, the Company acquired full development and commercialization rights globally, with the exception of Greater China, for $3,500. The Company accounted for the transaction as an asset acquisition as substantially all of the fair value of the assets acquired was concentrated in a single identified asset. In March 2023, the Company achieved a preclinical milestone, which triggered a $750 payment under the provisions of the APA, which the Company recognized as an IPR&D charge recorded in research and development within the unaudited condensed consolidated statement of operations and comprehensive income for the nine months ended September 30, 2023. There are additional payments due under the APA upon the achievement of certain milestones including $1,000 for preclinical milestones, $19,000 for development milestones, $44,000 for regulatory milestones and $110,000 for sales milestones.

13

9. ACCRUED EXPENSES

Accrued expenses consist of the following:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Royalties due to Bioprojet

$

29,665

$

25,367

Rebates and other sales deductions

 

31,853

 

27,860

Interest

3,140

3,286

Selling and marketing

 

2,253

 

1,135

Research and development

 

2,190

 

358

Professional fees, consulting, and other services

 

1,841

 

1,163

Other expenses

 

1,819

 

773

$

72,761

$

59,942

10. DEBT

Term Loan A Credit Agreement

On July 26, 2023, the Company entered into a Credit Agreement (the “TLA Credit Agreement”) with JPMorgan Chase Bank, N.A., as “Administrative Agent”, and certain lenders. The TLA Credit Agreement provides for a five-year senior secured term loan (the “TLA Term Loan”) in an aggregate principal amount of $185,000.

On September 21, 2023, the Company entered into the First Incremental Amendment (the “First Incremental Amendment”) with the Administrative Agent and Bank of America, N.A., as incremental lender. The First Incremental Amendment provides for an incremental senior secured term loan (the “Incremental Term Loan”) in an aggregate principal amount of $15,000. The First Incremental Amendment amends the TLA Credit Agreement and provides that the Incremental Term Loan will have identical terms as the TLA Term Loan.

The repayment schedule for both the TLA Term Loan and the Incremental Term Loan (together, the “Term Loans”) consists of quarterly $3,750 principal payments, which commence on December 31, 2023, increasing to quarterly $5,000 principal payments beginning on December 31, 2025, with a $115,000 payment due on the maturity date of July 26, 2028. The Term Loans bear interest at a per annum rate equal to, at the Company’s option, (i) a base rate plus a specified margin ranging from 2.50% to 3.00%, based on the Company’s senior secured net leverage ratio (as defined in the TLA Credit Agreement) or (ii) Term SOFR plus a credit spread adjustment of 0.10% plus a specified margin ranging from 3.50% to 4.00%, based on the Company’s senior secured net leverage ratio.

The net cash received related to the Term Loans as a result of the transactions, less debt issuance costs of $2,997, was $197,003. The debt issuance costs related to the Term Loans will be amortized as additional interest expense over the loan term of the TLA Credit Agreement. The fair value of the Term Loans as of September 30, 2023 was $199,820.

14

Blackstone Credit Agreement

In August 2021, the Company entered into the Blackstone Credit Agreement that provided for (i) a senior secured term loan facility in an aggregate original principal amount of $200,000 (the “Initial Term Loan”) and (ii) a senior secured delayed draw term loan facility in an aggregate principal amount up to $100,000 (the “DDTL”). The DDTL was initially available to draw down through August 9, 2022. In August 2022, the Company entered into an agreement to extend the expiration date of the DDTL to August 9, 2023, for which the Company would pay a ticking fee at a rate of 1% per annum on the undrawn portion of the DDTL (the “Ticking Fee”), which commenced on August 10, 2022.

Net cash received from the Initial Term Loan was $191,849, net of debt issuance costs of $8,151. In addition, the Company paid $1,000 in debt issuance costs relating to the DDTL, which was initially recorded in other current assets within the unaudited condensed consolidated balance sheet.

In connection with the TLA Credit Agreement, the Company extinguished the Blackstone Credit Agreement, which required a payoff amount of $207,308 consisting of principal repayment, interest, exit fees, Ticking Fee and a prepayment premium. The Company recognized a loss on extinguishment of debt of $9,766 relating to the Blackstone Credit Agreement within the Company’s unaudited condensed consolidated statements of operation and comprehensive income for the three and nine months ended September 30, 2023. In addition, the Company recognized $1,972 relating to unamortized debt issuance costs relating to the DDTL and the Ticking Fee, which was recorded in interest expense, net within the unaudited condensed consolidated statement of operations and comprehensive income for the three and nine months ended September 30, 2023.

Long-term debt, net consists of the following:

    

September 30, 

    

December 31, 

2023

2022

Liability component - principal

$

200,000

$

197,500

Unamortized debt discount associated with debt financing costs

 

(2,869)

 

(5,853)

Liability component - net carrying value

197,131

191,647

Less current portion

(15,000)

(2,000)

Long-term debt, net

$

182,131

$

189,647

15

Future minimum payments relating to long-term debt, net as of September 30, 2023, for the periods indicated below consists of the following:

Years ending December 31, 

2023 (Excluding the nine months ended September 30, 2023)

$

3,750

2024

 

15,000

2025

 

16,250

2026

 

20,000

2027

 

20,000

Thereafter

125,000

Total

$

200,000

Interest expense related to the Company’s long-term debt, net, is included in interest expense, net in the unaudited condensed consolidated statements of operations and comprehensive income and consists of the following:

Three Months Ended

Nine Months Ended

September 30, 

September 30, 

2023

    

2022

2023

    

2022

Interest on principal balance

$

4,791

$

4,513

$

15,900

$

12,110

Amortization of deferred financing costs

 

2,221

 

418

 

3,061

 

1,241

Total term loan interest expense

$

7,012

$

4,931

$

18,961

$

13,351

11. LEASES

In June 2018, the Company entered into an operating lease for approximately fifteen thousand square feet of office space in Plymouth Meeting, PA, which expires in May 2024. The Company subsequently entered into two separate operating leases for additional office space in Plymouth Meeting, PA, which include approximately thirteen thousand square feet and seven thousand square feet of additional office space, respectively, and expire in May 2024. The terms of the lease payments provide for rental payments on a monthly basis and on a graduated scale. The Company also leases a fleet of automobiles that are used by its sales representatives and are classified as operating leases.

Operating lease right-of-use assets and operating lease liabilities are recognized based on the present value of the future lease payments using our incremental borrowing rate. Leases with an initial term of 12 months or less are not recorded on the balance sheet. Our leases have remaining lease terms of less than 1 year to 3 years, some of which may include the option to extend or terminate the leases.

The Company recorded operating lease costs of $473 and $378 for the three months ended September 30, 2023 and 2022, respectively, and $1,295 and $1,155 for the nine months ended September 30, 2023 and 2022, respectively.

As of September 30, 2023, the weighted-average remaining lease term for operating leases was 1.8 years and the weighted-average discount rate for operating leases was 6.0%.

16

Supplemental balance sheet information related to operating leases was as follows:

Leases

Classification

September 30, 2023

  

December 31, 2022

Assets

Operating lease right-of-use assets

Other noncurrent assets

$

2,456

$

2,312

Liabilities

Operating lease liability, current portion

Other current liabilities

$

1,683

$

1,614

Operating lease liability, long-term

Other long-term liabilities

901

975

Total operating lease liabilities

$

2,584

$

2,589

Supplemental cash flow information related to operating leases was as follows:

September 30, 2023

September 30, 2022

Operating cash flows from operating leases

$

1,448

$

1,297

Right of use assets obtained in exchange for operating lease obligations

$

1,592

$

485

Future payments under noncancelable operating leases with initial terms of one year or more as of September 30, 2023 consisted of the following:

Years ending December 31, 

    

2023 (Excluding the nine months ended September 30, 2023)

$

558

2024

 

1,407

2025

 

532

2026

 

252

2027

 

Thereafter

 

Total lease payments

2,749

Less: imputed interest

(165)

Total lease liabilities

$

2,584

12. COMMITMENTS AND CONTINGENCIES

Litigation

From time to time, the Company is subject to claims and suits arising in the ordinary course of business. The Company accrues such liabilities when they are known, if they are deemed probable and can be reasonably estimated. As of September 30, 2023, there were no material claims or suits outstanding.

13. STOCKHOLDERS’ EQUITY

Common Stock

The holders of common stock are entitled to one vote for each share held on all matters submitted to a vote of the Company’s stockholders. The holders of common stock do not have any cumulative voting rights. Holders of common stock are entitled to receive ratably any dividends declared by the Company’s board of directors out of funds legally available for that purpose, subject to any preferential dividend rights of any outstanding preferred stock. The Company’s common stock has no preemptive rights, conversion rights or other subscription rights or redemption or sinking fund provisions.

17

Share Repurchase Program

On August 1, 2023, the Company’s Board of Directors approved a program providing for the repurchase of shares of common stock in an aggregate amount of up to $125,000, excluding commissions and transaction fees (the “August 2023 Repurchase Program”). The August 2023 Repurchase Program may be suspended, terminated or modified at any time for any reason. During the three and nine months ended September 30, 2023, the Company repurchased and cancelled 1,439,792 shares of common stock at an aggregate cost of $50,000, exclusive of commissions and transaction fees. As of September 30, 2023 the remaining amount of common stock authorized for repurchases was $75,000.

See Note 18 to our unaudited condensed consolidated financial statements for information related to the termination of the August 2023 Repurchase Program as of October 27, 2023.

14. STOCK INCENTIVE PLAN AND STOCK-BASED COMPENSATION

2020 Stock Incentive Plan

In connection with the Company’s IPO, the board of directors adopted, and its stockholders approved, the 2020 Incentive Award Plan (the “2020 Plan”), in order to facilitate the grant of cash and equity incentives to directors, employees (including the Company’s named executive officers) and consultants of the Company and its subsidiaries. The 2020 Plan provides for the grant of stock options, including incentive stock options (“ISOs”) and non-qualified stock options (“NSOs”), SARs, restricted stock, dividend equivalents, restricted stock units (“RSUs”) and other stock or cash-based awards.

Stock options and stock appreciation rights under the 2020 Plan have a 10-year contractual term and vest over the vesting period specified in the applicable award agreement, at achievement of a performance requirement, or upon change of control (as defined in the applicable plan). RSUs vest over the vesting period specified in the applicable award agreement, at achievement of a performance requirement, or upon change of control (as defined in the applicable plan). As of September 30, 2023, there were 6,755,091 shares of common stock available for issuance under the 2020 Plan. The number of shares that may be issued under the 2020 Plan will automatically increase on January 1 of each year in an amount equal to the lesser of (i) 4.0% of the shares of the Company’s common stock outstanding on December 31 of the preceding year or (ii) an amount determined by the Company’s board of directors.

2017 Stock Incentive Plan

In August 2017, the Company adopted an equity incentive plan (the “2017 Plan”). Under the 2017 Plan, directors, officers, employees, consultants, and advisors of the Company can be paid incentive compensation measured by the value of the Company’s shares of common stock through grants of stock options, stock appreciation rights (“SARs”), or restricted stock. Following the adoption of the 2020 Plan, no further grants have been, or will be, made under the 2017 Plan. However, the 2017 Plan will continue to govern the terms and conditions of outstanding awards granted under it.

18

Stock Options

The following table summarizes stock option activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Exercise

Contractual

    

Awards

    

Price

    

Term

Awards outstanding—December 31, 2022

 

6,460,947

$

30.90

 

7.86

Awards issued

 

376,422

$

36.71

 

  

Awards exercised

 

(367,376)

$

12.02

 

  

Awards forfeited

 

(206,318)

$

24.84

 

  

Awards outstanding—September 30, 2023

 

6,263,675

$

32.55

 

7.39

Stock Appreciation Rights

The following table summarizes SARs activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Exercise

Contractual

    

Awards

    

Price

    

Term

Awards outstanding—December 31, 2022

 

43,208

$

9.38

 

6.32

Awards issued

 

$

 

  

Awards exercised

 

$

 

  

Awards forfeited

 

$

 

  

Awards outstanding—September 30, 2023

 

43,208

$

9.38

 

5.58

Restricted Stock Units

The following table summarizes RSU activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Grant Date

Contractual

    

Awards

    

Fair Value

    

Term

Awards outstanding—December 31, 2022

 

60,000

$

29.03

 

8.24

Awards issued

 

$

 

  

Awards vested

 

(30,000)

$

29.03

 

  

Awards forfeited

 

$

 

  

Awards outstanding—September 30, 2023

 

30,000

$

29.03

 

7.49

As of September 30, 2023 and December 31, 2022, stock awards issued under the 2017 and 2020 Plans of 3,141,836 and 1,818,045 shares of common stock, respectively, were vested.

Value of Stock Options and SARs

The Company values options and SARs using the Black-Scholes option-pricing model. The Company lacks sufficient historical company-specific volatility information. Therefore, the Company estimates expected stock volatility based on historical volatility of peer companies and expects to continue to do so until such time as it has adequate historical data regarding the volatility of its own traded stock price. For options with service-

19

based vesting conditions, the expected term of the Company’s stock options has been determined utilizing the “simplified” method for awards that qualify as “plain-vanilla” options. For SARs, the expected term is based upon the weighting of certain future events. The risk-free interest rate is determined by reference to the U.S. Treasury yield curve in effect at the time of grant of the award for the time periods approximately equal to the expected term of the award. An expected dividend yield of 0% is based on the fact that the Company has never paid cash dividends and does not expect to do so in the foreseeable future.

The assumptions used to value the awards are summarized in the following table.

As of

    

September 30, 

    

December 31, 

    

2023

    

2022

Dividend yield

 

0.00

%  

0.00

%

Expected volatility

 

76.32 - 80.21

%  

72.57 - 77.08

%

Risk-free interest rate

 

3.42 - 4.61

%  

1.99 - 4.05

%

Lack of marketability discount

 

0.00

%  

0.00

%

Expected term (years)

 

2.4 - 6.3

 

3.1 - 6.3

Value of RSUs

The fair value of RSUs is equal to the value of the Company’s common stock on the grant date.

The weighted average per share fair value of awards issued under the 2017 Plan and 2020 Plan was $20.13 and $18.88 on September 30, 2023 and December 31, 2022, respectively.

Stock-Based Compensation Expense

Stock-based compensation expense, net for the three and nine months ended September 30, 2023 and 2022, was recorded in the unaudited condensed consolidated statements of operations and comprehensive income in the following line items:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

    

2023

    

2022

    

2023

    

2022

Research and development expense

$

1,030

$

522

$

2,962

$

1,866

Sales and marketing expense

 

1,218

 

1,096

 

3,437

 

2,956

General and administrative expense

 

5,709

 

5,349

 

15,912

 

14,412

$

7,957

$

6,967

$

22,311

$

19,234

Stock-based compensation expense, net related to options and RSUs issued under the 2017 Plan and 2020 Plan is included in stockholder’s equity, and a liability for SARs is included in other non-current liabilities, in the Company’s unaudited condensed consolidated balance sheet. As of September 30, 2023, the total unrecognized stock-based compensation expense related to options and RSUs was $67,842. Such amount will be recognized in the Company’s consolidated statement of operations over a weighted average period of 2.4 years.

Employee Stock Purchase Plan

The 2020 Employee Stock Purchase Plan (“ESPP”) was adopted by the Company’s Board of Directors on April 30, 2021. The ESPP permits eligible employees to purchase shares of the Company’s common stock at a 15% discount from the lesser of the fair market value per share of the Company’s common stock on the first day of the offering period or the fair market value of the Company’s common stock on the purchase date. Funds are collected from employees through after-tax payroll deductions. The total number of shares reserved for issuance under the ESPP was initially 629,805, which will automatically increase on January 1 of each year in an amount equal to the lesser of (i) 1.0% of the shares of the Company’s common stock outstanding on

20

December 31 of the preceding year or (ii) an amount determined by the Company’s board of directors. It is intended that the ESPP meet the requirements for an “employee stock purchase plan” under Section 423 of the Internal Revenue Code. There were no shares issued under the ESPP for the three months ended September 30, 2023 and 2022, and there were 14,043 and 14,889 shares issued under the ESPP for the nine months ended September 30, 2023 and 2022, respectively. The discount on the ESPP was $100 and $86 for the three months ended September 30, 2023 and 2022, respectively, and $308 and $271 for the nine months ended September 30, 2023 and 2022, respectively, and is recorded within stock-based compensation expense.

15. EARNINGS PER SHARE

Basic earnings per share is calculated by dividing net income by the weighted average number of shares of common stock outstanding. Diluted net income per share of common is computed under the treasury stock method by using the weighted average number of shares of common stock outstanding, plus, for periods with net income, the potential dilutive effects of stock options, stock appreciation rights and restricted stock units.

The following table sets forth the computation of basic and diluted net income per share:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Numerator

 

  

 

  

  

 

  

Net income

$

38,461

$

87,943

$

102,246

$

132,959

Denominator

 

  

 

  

 

  

 

  

Net income per share of common stock - basic

$

0.64

$

1.48

$

1.71

$

2.25

Net income per share of common stock- diluted

$

0.63

$

1.44

$

1.68

$

2.18

Weighted average number of shares of common stock - basic

 

59,863,102

 

59,234,720

 

59,856,941

 

59,070,063

Weighted average number of shares of common stock - diluted

 

60,681,676

 

61,207,625

 

60,892,992

 

60,921,482

Securities outstanding that were included in the computation above, utilizing the treasury stock method are as follows:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Stock options, SARs, and RSUs to purchase common stock

818,574

1,972,905

1,036,051

1,851,419

Potential shares of common stock issuable that were excluded from the computation of diluted weighted-average shares outstanding excluded from the numerator, are as follows:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Stock options, SARs, and RSUs to purchase common stock

 

5,518,309

 

4,754,958

5,300,832

 

4,876,444

21

16. INCOME TAXES

A reconciliation between the statutory federal income tax rate and the Company’s effective income tax rate for the three and nine months ended September 30, 2023 and 2022 is as follows:

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

2023

    

2022

 

Federal income tax rate

21.0

%  

21.0

%

21.0

%  

21.0

%

Stock-based compensation

(17.0)

(0.9)

4.4

State taxes

4.0

(22.1)

4.7

 

(0.5)

Credits

0.2

(1.6)

(0.2)

Other

0.6

0.3

 

0.7

Valuation allowance

(985.7)

 

(144.9)

Total

25.8

%  

(1,003.8)

%

23.5

%  

(119.5)

%

17. RELATED-PARTY TRANSACTIONS

The Company was party to a management agreement for professional services provided by a related party, Paragon Biosciences, LLC (“Paragon”). The related party is an entity that shares common ownership with the Company. In addition, the Chairman of the Company’s board of directors was the President and owner of the entity. The Company terminated the management agreement upon the consummation of its IPO. The Company is also party to a right of use agreement with the related party whereby it has access to and the right to use certain office space leased by the related party in Chicago, IL. In addition, the Company had participated in certain transactions with separate related parties that also share common ownership with the Company, primarily related to combined employee health plans. The Company incurred $73 and $71 for the three months ended September 30, 2023 and 2022, and incurred $218 and $213 for the nine months ended September 30, 2023 and 2022, respectively, in expenses to this related party, which are included in general and administrative expense in the unaudited condensed consolidated statements of operations and comprehensive loss. As of September 30, 2023 and December 31, 2022, there were no amounts due to or due from related parties included in the unaudited condensed consolidated balance sheets.

18. SUBSEQUENT EVENTS

On October 10, 2023, the Company completed a tender offer (the “Tender Offer”) to acquire all of the outstanding shares of common stock of Zynerba Pharmaceuticals, Inc. (“Zynerba Common Stock”), a clinical-stage pharmaceutical company focused on innovative pharmaceutically produced transdermal cannabidiol therapies for orphan neuropsychiatric disorders, including Fragile X syndrome.

Under the terms of the Tender Offer, the Company paid (i) $1.1059 per share of Zynerba Common Stock (the “Common Cash Amount”), plus (ii) one contingent value right (each, a “CVR”) per share of Zynerba Common Stock (the “Common CVR Amount”) for each holder of Zynerba Common Stock upon the closing of the Tender Offer, which represents the right to receive up to approximately $2.5444 per share of Zynerba Common Stock, subject to the achievement of certain clinical, regulatory and sales-based milestones. Both the Common Cash Amount and Common CVR Amount are to be paid in cash, subject to any applicable withholding of taxes and without interest. The aggregate consideration paid by the Company to acquire the Zynerba Common Stock upon completion of the Tender Offer was $60,000, exclusive of transaction related fees. The Company financed the acquisition with cash on hand.

On October 27, 2023, the Company’s Board of Directors approved a program providing for the repurchase of shares of common stock in an aggregate amount of up to $200,000, excluding commissions and transaction fees (the “October 2023 Repurchase Program”). The board simultaneously terminated the August 2023 Repurchase Program and any remaining amount authorized for the repurchase of shares. The October 2023 Repurchase Program may be suspended, terminated, or modified at any time for any reason.

22

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.

Cautionary Note Regarding Forward-Looking Statements

This Quarterly Report on Form 10-Q contains forward-looking statements. We intend such forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in Section 27A of the Securities Act of 1933, as amended (the “Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended (the “Exchange Act”). All statements other than statements of historical facts contained in this Quarterly Report on Form 10-Q, including statements regarding our future results of operations and financial position, business strategy, products, prospective products, product approvals, research and development costs, anticipated timing and likelihood of success of clinical trials, expected timing of the release of clinical trial data, the plans and objectives of management for future operations and future results of anticipated products, are forward-looking statements. These statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Important factors that could cause such differences include, but are not limited to, statements about:

our commercialization efforts and strategy for WAKIX;
the rate and degree of market acceptance and clinical utility of pitolisant in additional indications, if approved, and any other product candidates we may develop or acquire, if approved;
our research and development plans, including our plans to explore the therapeutic potential of pitolisant in additional indications;
our ongoing and planned clinical trials;
our ability to expand the scope of our license agreements with Bioprojet Société Civile de Recherche (Bioprojet);
the availability of favorable insurance coverage and reimbursement for WAKIX;
the timing of, and our ability to obtain, regulatory approvals for pitolisant for other indications as well as any other product candidates;
our estimates regarding expenses, future revenue, capital requirements and additional financing needs;
our ability to identify, acquire and integrate additional products or product candidates with significant commercial potential that are consistent with our commercial objectives;
our commercialization, marketing and manufacturing capabilities and strategy;
significant competition in our industry;
our intellectual property position;
loss or retirement of key members of management;
failure to successfully execute our growth strategy, including any delays in our planned future growth;

23

our failure to maintain effective internal controls; and
the impact of government laws and regulations.

In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “expect,” “plan,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “potential”, or “continue” or the negative of these terms or other similar expressions. The forward-looking statements in this Quarterly Report on Form 10-Q are only predictions. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition and results of operations. These forward-looking statements speak only as of the date of this Quarterly Report on Form 10-Q and are subject to a number of important factors that could cause actual results to differ materially from those in the forward-looking statements, including the factors described under the section in our most recent Annual Report on Form 10-K entitled “Item 1A. Risk Factors” and the sections in this Quarterly Report on Form 10-Q titled “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations.”

Moreover, we operate in an evolving environment. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties.

Unless otherwise indicated, information contained in this Quarterly Report on Form 10-Q concerning our industry, including industry statistics and forecasts, competitive position and the markets in which we operate is based on information from independent industry and research organizations, other third-party sources and management estimates. Management estimates are derived from publicly available information released by independent industry analysts and other third-party sources, as well as data from our internal research, and are based on assumptions made by us upon reviewing such data, and our experience in, and knowledge of, such industry and markets, which we believe to be reasonable. In addition, projections, forecasts, assumptions and estimates of the future performance of the industry in which we operate and our future performance are necessarily subject to uncertainty and risk due to a variety of factors, including those described in “Risk Factors” and “Cautionary Note Regarding Forward-Looking Statements.” These and other factors could cause results to differ materially from those expressed and forecasts in the estimates made by the independent parties and by us.

You should read this Quarterly Report on Form 10-Q and the documents that we reference in this Quarterly Report on Form 10-Q completely and with the understanding that our actual future results may be materially different from what we expect. We qualify all of our forward-looking statements by these cautionary statements. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

As used herein, the terms “Harmony,” “we,” “us,” “our” and “the Company” refer to Harmony Biosciences Holdings, Inc., a Delaware corporation and our operating subsidiary, Harmony Biosciences, LLC.

Further, we have in-licensed from Bioprojet the registered trademark product name WAKIX® in the United States. We also have registered trademark protection in the United States for KNOW NARCOLEPSY®, REM AT THE WRONG TIME® and NON-REM AT THE WRONG TIME®, as well as our brand and logo HB®, HB HARMONY BIOSCIENCES® and HARMONY BIOSCIENCES®. This report also includes trademarks, service marks and trade names of other companies. Trademarks, service marks and trade names appearing in this Quarterly Report on Form 10-Q are the property of their respective owners.

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Company Overview

We are a commercial-stage, pharmaceutical company focused on developing and commercializing innovative therapies for patients living with rare neurological diseases as well as patients living with other neurological who have unmet medical needs. Our product, WAKIX (pitolisant), is a first-in-class molecule with a novel mechanism of action (“MOA”) specifically designed to increase histamine signaling in the brain by binding to H3 receptors. In August 2019, WAKIX was approved by the U.S. Food and Drug Administration (the “FDA”) for the treatment of excessive daytime sleepiness (“EDS”) in adult patients with narcolepsy, and its U.S. commercial launch was initiated in November 2019. In October 2020, WAKIX was approved by the FDA for the treatment of cataplexy in adult patients with narcolepsy. WAKIX is the first-and-only approved product for patients with narcolepsy that is not scheduled as a controlled substance by the U.S. Drug Enforcement Administration (the “DEA”).

We believe that pitolisant’s ability to regulate histamine gives it the potential to provide therapeutic benefit in other rare neurological diseases that are mediated through H3 receptors and histamine signaling. We are taking a mechanism-based approach to managing the life cycle of pitolisant and identified idiopathic hypersomnia (“IH”), another central disorder of hypersomnolence like narcolepsy, as our next potential new indication for WAKIX, which received Orphan Drug designation by the FDA in September 2023. In April 2022, we initiated a Phase 3 registrational trial, the INTUNE Study, to evaluate the efficacy and safety of pitolisant in adult patients with IH. We completed enrollment in the INTUNE study in May 2023 and we announced topline data on October 11, 2023. While the primary endpoint did not meet statistical significance, the totality of the data showed favorable trends for pitolisant in the treatment of adult patients with IH. We are currently analyzing the full data set to determine next steps, which include interactions with the FDA. We are focusing our development efforts on other rare neurological disorders in which EDS is a prominent symptom, including Prader-Willi Syndrome (“PWS”) and myotonic dystrophy, otherwise known as dystrophia myotonica (“DM”). Based on the positive signals from the data from our Phase 2 proof-of-concept signal detection clinical trial to evaluate pitolisant for the treatment of EDS and other key symptoms in patients with PWS, an end-of-phase 2 meeting with the FDA was held in June 2023. We aligned with the FDA on the proposed Phase 3 study design to support further investigation of pitolisant as a potential treatment to address the unmet medical need for children, adolescents and adults with PWS experiencing EDS, for which there is currently no approved treatment. In October 2023, we received FDA alignment of the protocol for the Phase 3 TEMPO study in patients with PWS, which will satisfy the requirements for both the registrational trial and pediatric exclusivity. We expect to initiate the Phase 3 study in the first quarter of 2024. In June 2021, we initiated a Phase 2 proof-of-concept clinical trial to evaluate pitolisant for the treatment of EDS, fatigue and cognitive dysfunction in adult patients with DM1 and we are on track for topline results from this trial in the fourth quarter of 2023.

Our partner, Bioprojet, completed a Phase 3 trial in pediatric patients with narcolepsy and received an approval from the European Medical Agency’s (“EMA”) Committee for Medicinal Products for Human Use (“CHMP”) for a pediatric narcolepsy indication. We are working with Bioprojet towards the submission to the FDA of a supplemental NDA for pediatric narcolepsy, which we plan to submit in the fourth quarter of 2023. In addition, we made progress with FDA in gaining alignment on the requirements for pediatric exclusivity for WAKIX, which we are actively pursuing.

We are actively working to expand our pipeline through the acquisition of additional assets that focus on addressing the unmet needs of patients living with rare neurological diseases as well as patients living with other neurological who have unmet medical needs. We are targeting assets that will allow us to further leverage the expertise and infrastructure that we have successfully built at Harmony so we can optimize the benefit of internal synergies. Consistent with this objective, in July 2022, we entered into a License and Commercialization Agreement (the “2022 LCA”) with Bioprojet whereby we obtained exclusive rights to manufacture, develop and commercialize one or more new products based on pitolisant in the United States and Latin America, with the potential to add additional indications and formulations upon the agreement of both parties. The 2022 LCA has the potential to generate new intellectual property and extend the pitolisant franchise. We are co-developing the new formulations of pitolisant with Bioprojet and work is ongoing. One of the formulations was dosed in a phase 1 pharmacokinetic study in healthy volunteers in October 2023.

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In addition, on October 10, 2023, we completed the acquisition of Zynerba Pharmaceuticals, Inc. (“Zynerba”), a clinical-stage pharmaceutical company focused on innovative pharmaceutically produced transdermal cannabidiol therapies for orphan neuropsychiatric disorders. Zynerba’s drug candidate is Zygel (also known as ZYN002), the first and only pharmaceutically-produced synthetic cannabidiol gel, devoid of THC, and formulated as a patent protected, permeation-enhanced gel for transdermal delivery. Zygel is currently in a pivotal Phase 3 study for the treatment of Fragile X Syndrome.

In August 2021, we entered into an asset purchase agreement with ConSynance Therapeutics, Inc. (the “APA”) to acquire HBS-102, a Melanin-concentrating hormone receptor 1 (MCHR1) antagonist previously developed as CSTI-100/ALB-127258(a)/ALB-127258 (the “Compound”), along with intellectual property and other assets related to the development, manufacture, and commercialization of the Compound. In connection with the acquisition, we made an upfront payment of $3.5 million and will be required to make additional payments upon the achievement of certain development milestones, regulatory milestones, and sales milestones and pay ongoing royalties upon commercialization. We acquired full development and commercialization rights globally, but we have provided a grant-back license to ConSynance for the development and commercialization of the Compound in Greater China. A preclinical proof-of-concept study to assess the effect of HBS-102 on hyperphagia, weight gain, and other metabolic parameters in a mouse model of PWS is ongoing. A thirteen week chronic toxicity study was initiated during the third quarter of 2023.

Pitolisant was developed by Bioprojet and approved by the EMA in 2016 for the treatment of narcolepsy in adult patients with or without cataplexy and in 2021 for the treatment of EDS in adult patients with obstructive sleep apnea. We acquired an exclusive license to develop, manufacture and commercialize pitolisant in the United States pursuant to our license agreement with Bioprojet (as amended, the “2017 LCA”) in July 2017. Pitolisant was granted Orphan Drug Designation for the treatment of narcolepsy by the FDA in 2010. It received Breakthrough Therapy designation for the treatment of cataplexy in patients with narcolepsy and Fast Track status for the treatment of EDS and cataplexy in patients with narcolepsy in April 2018.

We were founded in July 2017 as Harmony Biosciences II, LLC, a Delaware limited liability company. We converted to a Delaware corporation named Harmony Biosciences II, Inc. in September 2017, and, in February 2020, we changed our name to Harmony Biosciences Holdings, Inc. Our operations are conducted by our wholly owned subsidiary, Harmony Biosciences, LLC, which was formed in May 2017. Our operations to date have consisted of building and staffing our organization, acquiring the rights to pitolisant, raising capital, opening an investigational new drug application (“IND”) for pitolisant in narcolepsy, conducting an Expanded Access Program (“EAP”) for pitolisant for appropriate patients with narcolepsy in the United States, preparing and submitting our NDA for pitolisant, gaining NDA approval for WAKIX for the treatment of EDS or cataplexy in adult patients with narcolepsy, and launching and commercializing WAKIX in the United States. In addition, we have opened INDs for the development of pitolisant in PWS, DM and IH and have initiated clinical trials in pursuit of potential new indications in those rare disease patient populations.

Commercial Performance Metrics

As of September 30, 2023, we continued to see growth in the number of unique healthcare professional (“HCP”) prescribers of WAKIX since it became available in November 2019. The average number of patients on WAKIX for the three months ended September 30, 2023 was approximately 5,800. Additionally, as of September 30, 2023, we have secured formulary access for more than 80% of all insured lives (Commercial, Medicare and Medicaid) in the United States. Within these covered lives, we have observed favorable access to WAKIX subsequent to the expanded approval of WAKIX for the treatment of cataplexy in adult patients with narcolepsy in October 2020.

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Financial Operations Overview

Revenue

Net product sales includes gross sales of WAKIX less provisions for sales discounts and allowances, which includes trade allowances, rebates to government and commercial entities, and discounts. Although we expect net sales to increase over time, provisions for sales discounts and allowances may fluctuate based on the mix of sales to different customer segments and/or changes in our estimates.

Cost of Product Sales

Cost of product sales includes manufacturing and distribution costs, the cost of the drug substance, FDA program fees, royalties due to third parties on net product sales, freight, shipping, handling, storage costs and salaries of employees involved with production. We expect the cost of product sales to increase as we continue to ramp up production in order to meet future demand for WAKIX and diversify our supply chain for WAKIX.

The shelf life of WAKIX is three years from date of manufacture, with the earliest expiration of current inventory expected to be January 2025. We regularly review our inventory levels and expect write-offs from time to time. We will continue to assess inventory levels in future periods as demand for WAKIX and the rate of inventory turnover evolves. We currently expect to have adequate supply of WAKIX into the first quarter of 2025, with additional API on-hand inventory to support at least 36 months beyond this time frame.

Research and Development Expenses

Research and development expenses primarily include development programs for potential new indications for pitolisant in patients with IH, PWS and DM. We also incur research and development expenses related to our team of Medical Science Liaisons (“MSLs”) who interact with key opinion leaders, with a focus on the science, the role of histamine in sleep-wake state stability and the novel mechanism of action of pitolisant. In addition, our MSLs support our market access team with the presentation of clinical data to payors upon request and our clinical development team to identify potential clinical trial sites. Research and development costs are expensed as incurred. We have significantly increased our research and development efforts as we advance our clinical programs in IH, PWS and DM and assess other product candidates to expand our pipeline. Research and development expenses also include:

employee-related expenses, such as salaries, share-based compensation, benefits and travel expenses for our research and development personnel;
direct third-party costs such as expenses incurred under agreements with CROs, and contract manufacturing organizations (CMOs);
manufacturing costs in connection with producing materials for use in conducting clinical trials;
costs related to packaging and labeling of clinical supplies;
other third-party expenses (e.g., consultants, advisors) directly attributable to the development of our product candidates; and
amortization expense for assets used in research and development activities.

We do not track research and development expenses on an indication-by-indication basis. A significant portion of our research and development costs are external costs, such as fees paid to CROs and CMOs,

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central laboratories, contractors, and consultants in connection with our clinical development programs. Internal expenses primarily relate to personnel who are deployed across multiple programs.

Product candidates in later stages of clinical development generally have higher development costs than those in earlier stages of clinical development, primarily due to the increased size and duration of later-stage clinical trials, milestone payments, and the cost of submitting an NDA to the FDA (and/or other regulatory authorities). We expect our research and development expenses to be significant over the next several years as we advance our current clinical development programs and prepare to seek regulatory approval for additional indications for pitolisant, advance HBS-102 from preclinical studies into the clinic, and identify potential new product candidates to develop toward new indications.

At this time, we cannot reasonably estimate or know the nature, timing and estimated costs of the efforts that will be necessary to complete the development of any additional indications for pitolisant or other product candidates that we move forward for regulatory approval. There are numerous risks and uncertainties associated with developing product candidates, including uncertainty related to:

the duration, costs and timing of clinical trials of our current development programs and any further clinical trials related to new product candidates;
the sufficiency of our financial and other resources to complete the necessary preclinical studies and clinical trials;
the impact of the COVID-19 pandemic, including any future resurgence or new variants, on the ability to initiate new clinical trials and/or maintain the continuity of ongoing clinical trials, including our ability to access sleep labs in order to conduct objective sleep testing, that could be impacted by future shelter-in-place orders and needs of the health care system to focus on managing patients affected by COVID-19;
receiving Bioprojets consent to pursue additional indications for pitolisant;
the acceptance of INDs for our planned clinical trials or future clinical trials;
the successful and timely enrollment and completion of clinical trials;
the successful completion of preclinical studies and clinical trials;
successful data from our clinical programs that support an acceptable risk-benefit profile of our product candidates in the intended populations;
the receipt and maintenance of regulatory and marketing approvals from applicable regulatory authorities;
establishing agreements with third-party manufacturers for clinical supply for our clinical trials and commercial manufacturing, if our product candidate is approved;
the entry into collaborations to further the development of our product candidates;
obtaining and maintaining patent and trade secret protection or regulatory exclusivity for our product candidates; and
successfully launching our product candidates and achieving commercial sales, if and when approved.

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A change in the outcome of any of these variables with respect to the development of any of our programs or any product candidate we develop would significantly change the costs, timing and viability associated with the development and/or regulatory approval of such programs or product candidates.

Sales and Marketing Expenses

Our sales and marketing expenses primarily relate to the market development and commercialization activities of WAKIX for the treatment of EDS and cataplexy in adult patients with narcolepsy. Market development and commercial activities account for a significant portion of our operating expenses and are expensed as incurred. We expect our sales and marketing expenses to increase in the near- and mid-term to support WAKIX’s indications for the treatment of EDS or cataplexy in adult patients with narcolepsy and to expand our portfolio with the anticipated growth from potential additional indications.

Sales and marketing expenses include:

employee-related expenses, such as salaries, share-based compensation, benefits and travel expenses for our sales, marketing and market access personnel;
healthcare professional-related expenses, including marketing programs, healthcare professional promotional medical education, disease education, conference exhibits and market research;
patient-related expenses, including patient awareness and education programs, disease awareness education, patient reimbursement programs, patient support services and market research;
market access expenses, including payor education, specialty pharmacy programs and services to support the continued commercialization of WAKIX; and
secondary data purchases (i.e., patient claims and prescription data), data warehouse development and data management.

In addition, sales and marketing expenses include external costs such as website development, media placement fees, agency fees for patient, medical education and promotional expenses, market research, analysis of secondary data, conference fees and consulting fees.

General and Administrative Expenses

General and administrative expenses consist primarily of employee-related expenses, such as salaries, share-based compensation, benefits and travel expenses for our personnel in executive, legal, finance and accounting, human resources, investor relations, and other administrative departments. General and administrative expenses also consist of office leases, and professional fees, including legal, tax and accounting and consulting fees.

We anticipate that our general and administrative expenses will increase in the future to support our continued commercialization efforts, ongoing and future potential research and development activities, and increased costs of operating as a public company. These increases will likely be driven by costs associated with the hiring of additional personnel and fees paid to outside consultants, lawyers and accountants, among other expenses. Additionally, we anticipate increased costs associated with being a public company, including expenses related to services associated with maintaining compliance with the requirements of Nasdaq and the SEC, insurance and investor relations costs. If any of our current or future indication expansion programs or new product candidates obtain U.S. regulatory approval, we expect that we would incur significantly increased expenses associated with building a sales and marketing team.

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Paragon Agreements

We were party to a management services agreement with Paragon Biosciences, LLC (“Paragon”), which was terminated upon the consummation of our IPO, pursuant to which Paragon provided us with certain professional services.

We are also party to a right-of-use agreement with Paragon whereby we have access to and the right to use certain office space leased by Paragon in Chicago, Illinois. For the three and nine months ended September 30, 2023, we paid fees of $0.1 million and $0.2 million, respectively, pursuant to this agreement.

Loss on Debt Extinguishment

Loss on debt extinguishment consists primarily of costs of extinguishment of debt during the applicable period related to the prepayment of our credit agreements.

Interest Expense, Net

Interest expense, net consists primarily of interest expense on debt facilities, amortization of debt issuance costs and amortization of premiums on our debt securities, partially offset by interest income earned on our cash and investment balances and accretion of the discount on our debt securities.

Results of Operations

The following table sets forth selected items in our unaudited condensed consolidated statements of operations for the periods presented:

Three Months Ended September 30, 

Nine Months Ended September 30, 

    

2023

    

2022

    

2023

    

2022

(In thousands)

(In thousands)

Net product revenues

$

160,268

$

117,206

$

413,610

$

309,547

Cost of product sales

 

32,296

 

22,959

 

78,084

 

56,596

Gross profit

 

127,972

 

94,247

 

335,526

 

252,951

Operating expenses:

 

  

 

  

 

  

 

  

Research and development

 

17,499

 

40,548

 

45,757

 

60,794

Sales and marketing

 

23,418

 

20,467

 

70,518

 

58,210

General and administrative

 

22,546

 

21,331

 

67,417

 

61,374

Total operating expenses

 

63,463

 

82,346

 

183,692

 

180,378

Operating income

 

64,509

 

11,901

 

151,834

 

72,573

Loss on debt extinguishment

 

(9,766)

 

 

(9,766)

 

Other (expense) income, net

 

(5)

 

56

 

(34)

 

96

Interest expense, net

 

(2,906)

 

(3,990)

 

(8,327)

 

(12,086)

Net income before provision for income taxes

 

51,832

 

7,967

 

133,707

 

60,583

Income tax (expense) benefit

 

(13,371)

 

79,976

 

(31,461)

 

72,376

Net income

$

38,461

$

87,943

$

102,246

$

132,959

Net Product Revenues

Net product revenues increased by $43.1 million, or 36.7%, for the three months ended September 30, 2023 and increased by $104.1 million, or 33.6%, for the nine months ended September 30, 2023, compared to the same periods in 2022. The increase for the three months ended September 30, 2023, was primarily due to a 28.2% increase in the number of units shipped, and the net impact of a 7.0% price increase. The increase for the nine months ended September 30, 2023, was primarily due to a 26.9% increase in number of units shipped,

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and the net impact of a 7.0% price increase. The price increase for both comparable periods occurred in January 2023.

Cost of Product Sales

Cost of product sales increased by $9.3 million, or 40.7%, for the three months ended September 30, 2023 and increased by $21.5 million, or 38.0%, for the nine months ended September 30, 2023, compared to the same periods in 2022. Cost of product sales as a percentage of net product revenues was 20.2% and 18.9% for the three and nine months ended September 30, 2023, respectively, compared to 19.6% and 18.3% for the three and nine months ended September 30, 2022, respectively. The increase in cost of product sales in both comparable periods was due to higher royalties as a result of higher sales of WAKIX and the increase in cost of product sales as a percentage of net product revenues was due to entering a higher royalty tier earlier in 2023 compared to 2022.

Research and Development Expenses

Research and development expenses decreased by $23.0 million, or 56.8%, for the three months ended September 30, 2023 and decreased by $15.0 million, or 24.7%, for the nine months ended September 30, 2023, compared to the same periods in 2022. The decrease for the three months ended September 30, 2023 was primarily driven by a $30 million licensing fee incurred upon entering the 2022 LCA with Bioprojet during the three months ended September 30, 2022, partially offset by a $5.7 million increase in clinical development work associated with IH, PWS and DM, a $0.9 million increase in personnel costs and a $0.5 million increase in stock compensation associated with new awards. The decrease for the nine months ended September 30, 2023 was primarily driven by a $30 million licensing fee incurred upon entering the 2022 LCA with Bioprojet during the nine months ended September 30, 2022, partially offset by an $11.0 million increase in clinical development work associated with IH, PWS and DM, a $2.3 million increase in personnel costs, a $1.1 million increase in stock compensation associated with new awards and a $0.8 million IPR&D charge related to preclinical milestones achieved for HBS-102.

Sales and Marketing Expenses

Sales and marketing expenses increased by $3.0 million, or 14.4%, for the three months ended September 30, 2023, and increased by $12.3 million, or 21.1%, for the nine months ended September 30, 2023, compared to the same periods in 2022. The increase for the three months ended September 30, 2023, was primarily due to a $2.3 million increase in personnel costs and a $0.4 million increase in patient engagement and marketing activities. The increase for the nine months ended September 30, 2023, was primarily due to a $7.1 million increase in patient engagement and marketing activities and a $4.8 million increase in personnel costs. The increase in patient engagement and marketing activities for both comparable periods was driven by our continued growth of WAKIX and the increase in personnel costs for both comparable periods was related to our sales force expansion.

General and Administrative Expenses

General and administrative expenses increased by $1.2 million, or 5.7%, for the three months ended September 30, 2023 and increased by $6.0 million, or 9.8%, for the nine months ended September 30, 2023, as compared to the same periods in 2022. The increase in the three months ended September 30, 2023 was primarily due to a $0.9 million increase in personnel costs and a $0.3 million increase in stock compensation associated with new awards. The increase in the nine months ended September 30, 2023 was primarily due to a $2.5 million increase in personnel costs, a $1.5 million increase to stock compensation associated with new awards and a $0.9 million increase in intangible asset amortization as a result of the $40.0 million milestone payment in March 2022 upon attaining $500.0 million in life-to-date aggregate net sales of WAKIX in the United States.

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Loss on Debt Extinguishment

Loss on debt extinguishment was $9.8 million for the three and nine months ended September 30, 2023.  There was no comparable amount in the prior year periods related to the extinguishment of the Blackstone Credit Agreement (defined below).

Interest Expense, Net

Interest expense, net decreased by $1.0 million, or 27.2%, for the three months ended September 30, 2023 and decreased by $3.8 million, or 31.1%, for the nine months ended September 30, 2023, compared to the same periods in 2022. The decrease for the three months ended September 30, 2023, was primarily due to a $2.6 million increase in interest income generated from our investments and cash equivalents, partially offset by $2.0 million in unamortized fees and ticking fees pertaining to the DDTL (defined below). The decrease for the nine months ended September 30, 2023, was primarily due to a $7.4 million increase in interest income generated from our investments and cash equivalents and a $2.0 million increase in accretion of discount on our investments, partially offset by a $3.8 million increase in interest expense due to higher rates and $2.0 million in unamortized fees and ticking fees pertaining to the DDTL (defined below).  

Income Taxes

Income tax expense was $13.4 million, representing a 25.8% effective tax rate, for the three months ended September 30, 2023, and $31.5 million, or an effective tax rate of 23.5%, for the nine months ended September 30, 2023. Income tax benefit was $80.0 million and $72.4 million for the three and nine months ended September 30. 2022, respectively. The income tax benefit related to both the three and nine months ended September 30, 2022 was due to the release of the valuation allowance on our deferred tax assets, partially offset by current period provision for state and federal income taxes. The effective tax rate of 23.5% for the nine months ended September 30, 2023 included 21.0% for the provision of federal income taxes and 4.7% for the provision of state income taxes, partially offset by a tax windfall benefit of 0.9% from the exercise of stock options and a 1.6% benefit from credits.

Liquidity, Sources of Funding and Capital Resources

Overview

To date, we have financed our operations primarily with (a) proceeds from sales of our convertible preferred stock; (b) borrowings under our debt agreements; (c) the proceeds from our IPO; and (d) the proceeds from the sale of common stock to Blackstone. From our inception through our IPO, we received aggregate proceeds of $345.0 million from sales of our convertible preferred stock. In August 2020, we completed the IPO of our common stock, in which we sold 6,151,162 shares of our common stock, including 802,325 shares of our common stock pursuant to the underwriters’ over-allotment option. The shares were sold at a price of $24.00 per share for net proceeds of approximately $135.4 million. As of September 30, 2023, we had cash, cash equivalents, restricted cash and investments of $438.6 million and an accumulated deficit of $169.9 million. As of September 30, 2023, we had outstanding debt of $200.0 million.

We have invested a portion of our available cash in money market funds, U.S. government and agency securities, corporate debt and commercial paper in accordance with our investment policy. Our investment policy defines allowable investments and establishes guidelines relating to credit quality, diversification, and maturities of our investments to preserve principal and maintain liquidity. All investment securities have a credit rating of at least A-2/P-2/F2 from at least two National Recognized Statistical Rating Organizations. Our investment portfolio may be adversely impacted by future disruptions in the credit markets.

The unaudited condensed consolidated financial statements have been prepared as though we will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business.

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We believe that our existing cash, cash equivalents and investments on hand as of September 30, 2023, will enable us to meet our operational liquidity needs and fund our planned investing activities for the next 12 months. We have based our liquidity and cash flow projections on assumptions that may prove to be incorrect, and we could use our capital resources sooner than we expect.

Term Loan A Credit Agreement

On July 26, 2023, we entered into a Credit Agreement (the “TLA Credit Agreement”) with JPMorgan Chase Bank, N.A., as “Administrative Agent”, and certain lenders. The TLA Credit Agreement provides for a five-year senior secured term loan (the “TLA Term Loan”) in an aggregate principal amount of $185.0 million.  

On September 21, 2023, we entered into the First Incremental Amendment (the “First Incremental Amendment”) with the Administrative Agent and Bank of America, N.A., as incremental lender. The First Incremental Amendment provides for an incremental senior secured term loan (the “Incremental Term Loan”) in an aggregate principal amount of $15.0 million. The First Incremental Amendment amends the TLA Credit Agreement and provides that the Incremental Term Loan will have identical terms as the TLA Term Loan.

The repayment schedule for both the TLA Term Loan and the Incremental Term Loan (together, the “Term Loans”) consists of $3.8 million quarterly principal payments, which commence on December 31, 2023, increasing to $5.0 million quarterly principal payments beginning on December 31, 2025, with a $115.0 million payment due on the maturity date of July 26, 2028. The Term Loans bear interest at a per annum rate equal to, at our option, (i) a base rate plus a specified margin ranging from 2.50% to 3.00%, based on our senior secured net leverage ratio (as defined in the TLA Credit Agreement) or (ii) Term SOFR plus a credit spread adjustment of 0.10% plus a specified margin ranging from 3.50% to 4.00%, based on our senior secured net leverage ratio.

The TLA Credit Agreement contains customary affirmative and negative covenants, financial covenants, representations and warranties, events of default and other provisions. We were in compliance with all covenants as of September 30, 2023.

Blackstone Credit Agreement

In August 2021, we entered into the Blackstone Credit Agreement that provided for (i) a senior secured term loan facility in an aggregate original principal amount of $200.0 million (the “Initial Term Loan”) and (ii) a senior secured delayed draw term loan facility in an aggregate principal amount up to $100.0 million (the “DDTL” and, together with the Initial Term Loans, the “Loans”). The DDTL was initially available to draw down through August 9, 2022. In August 2022, we entered into an agreement to extend the expiration date of the DDTL to August 9, 2023, for which we paid a ticking fee at a rate of 1% per annum on the undrawn portion of the DDTL, which commenced on August 10, 2022. We used substantially all of the proceeds from the Blackstone Credit Agreement, and the related sale of our common stock, to repay the balance of the OrbiMed Credit Agreement.

In connection with the TLA Credit Agreement, we extinguished the Blackstone Credit Agreement, which required a payoff amount of $207.3 million consisting of principal repayment, interest, exit fees, a ticking fee and a prepayment premium. We recognized a loss on extinguishment of debt of $9.8 million relating to the Blackstone Credit Agreement for the three and nine months ended September 30, 2023.

Share Repurchases

On August 1, 2023, our Board of Directors approved a program providing for the repurchase of shares of common stock in an aggregate amount of up to $125.0 million, excluding commissions and transaction fees. The repurchase program may be suspended, terminated or modified at any time for any reason. During the three and nine months ended September 30, 2023, we repurchased and cancelled 1,439,792 shares of common stock at an aggregate cost of $50.0 million, excluding commissions and transaction fees. As of September 30, 2023 the remaining amount of common stock authorized for repurchases was $75.0 million.

33

Acquisitions

On October 10, 2023, we completed a tender offer (the “Tender Offer”) to acquire all of the outstanding shares of common stock of Zynerba Pharmaceuticals, Inc. (“Zynerba Common Stock”).

Under the terms of the Tender Offer, we paid (i) $1.1059 per share of Zynerba Common Stock (the “Common Cash Amount”), plus (ii) one contingent value right (each, a “CVR”) per share of Zynerba Common Stock (the “Common CVR Amount”), which represents the right to receive up to approximately $2.5444 per share of Zynerba Common Stock, subject to the achievement of certain clinical, regulatory and sales-based milestones. Both the Common Cash Amount and Common CVR Amount are to be paid in cash, subject to any applicable withholding of taxes and without interest. The aggregate consideration we paid to acquire the Zynerba Common Stock upon completion of the Tender Offer was $60 million, exclusive of transaction related fees. We financed the acquisition with cash on hand.

Asset Purchase Agreement

In August 2021, we entered into the APA to acquire HBS-102, a potential first-in-class molecule with a novel mechanism of action. Under the terms of the agreement, we acquired full development and commercialization rights globally, with the exception of Greater China, for $3.5 million. Additionally, there are payments due upon the achievement of certain milestones, including $1.0 million for additional preclinical milestones (see “Recent Milestone Payments”), $19.0 million for development milestones, $44.0 million for regulatory milestones and $110.0 million for sales milestones.

License Agreement

In July 2022, we entered into the 2022 LCA with Bioprojet whereby we obtained exclusive rights to manufacture, develop and commercialize one or more new products based on pitolisant in the United States and Latin America, with the potential to add additional indications and formulations upon the agreement of both parties. We paid an initial, non-refundable $30.0 million licensing fee in October 2022 and additional payments of up to $155.0 million are potentially due under the 2022 LCA upon the achievement of certain future development and sales-based milestones. In addition, certain payments will become due upon the achievement of development milestones for new indications and formulations as agreed upon by both parties. The 2022 LCA also includes a fixed trademark royalty and a tiered royalty based on net sales of any new products commercialized, which will be payable to Bioprojet on a quarterly basis.

Recent Milestone Payments

In March 2023, we achieved a preclinical milestone, which triggered a $0.8 million payment under the provisions of the APA, which was paid in April 2023.  

In March 2022, we made a final $40.0 million milestone payment to Bioprojet upon WAKIX attaining $500.0 million in life-to-date aggregate net sales in the United States.

34

Cash Flows

The following table sets forth a summary of our cash flows for the nine months ended September 30, 2023 and 2022:

Nine Months Ended September 30, 

    

2023

    

2022

Selected cash flow data

(In thousands)

Cash provided by (used in):

 

  

 

  

Operating activities

$

142,722

$

117,788

Investing activities

 

(10,374)

 

(94,937)

Financing activities

 

(52,029)

 

4,183

Operating Activities

Net cash provided by operating activities for the nine months ended September 30, 2023 primarily consisted of net income of $102.2 million adjusted for non-cash items of $14.5 million related to deferred tax assets, $18.2 million related to intangible amortization and depreciation, $22.3 million related to stock-based compensation expense and $9.8 million related to loss on extinguishment of debt. Net working capital excluding cash increased by $3.4 million.

Net cash provided by operating activities for the nine months ended September 30, 2022 consisted of net income of $133.0 million adjusted for non-cash items of $81.7 million related to deferred tax assets, $17.3 million related to intangible amortization and depreciation and $19.2 million related to stock-based compensation expense. Net working capital excluding cash increased by $27.9 million, which was partially due to the accrual of the $30.0 million licensing fee associated with the 2022 LCA.

Investing Activities

Net cash used in investing activities for the nine months ended September 30, 2023 was $10.4 million, which was primarily attributable to $105.9 million in purchases of debt securities, partially offset by $95.7 million in proceeds from sales and maturities of investments and $0.2 million in purchases of property and equipment.

Net cash used in investing activities for the nine months ended September 30, 2022 was $94.9 million, which was primarily attributable to a final $40.0 million milestone payment associated with the 2017 LCA and $55.6 million in purchases of debt securities, partially offset by $0.9 million in proceeds from sales and maturities of investments.

Financing Activities

Net cash used in financing activities for the nine months ended September 30, 2023 was $52.0 million, which primarily consisted of $202.3 million in payments of principal and exit fees associated with the extinguishment of the Blackstone Credit Agreement, $50.0 million in share repurchases and $1.0 million in principal payments associated with the Blackstone Credit Agreement, partially offset by $197.0 million in proceeds associated with the TLA Credit Agreement, net of issuance costs, and $4.8 million in proceeds from exercised options.

Net cash provided by financing activities for the nine months ended September 30, 2022 was $4.2 million, which primarily consisted of $5.3 million in proceeds from exercised options partially offset by $1.5 million in principal payments associated with the Blackstone Credit Agreement.

35

Critical Accounting Estimates

Our management’s discussion and analysis of our financial condition and results of operations is based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America, or GAAP. The preparation of these financial statements requires us to make estimates, judgments and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities as of the dates of the balance sheets and the reported amounts of expenses during the reporting periods. In accordance with GAAP, we evaluate our estimates and judgments on an ongoing basis.

Significant estimates include assumptions used in the determination of the amount of revenue recognized on sales of WAKIX, our costs incurred under services type agreements related to the performance of research and development activities, and the measurement of compensation expense pursuant to stock-based awards. We base our estimates on contractual terms, historical experience and on various other factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.

We define our critical accounting policies as those under GAAP that require us to make subjective estimates and judgments about matters that are uncertain and are likely to have a material impact on our financial condition and results of operations, as well as the specific manner in which we apply those principles. During the quarter covered by this report, there were no material changes to the accounting policies and assumptions previously disclosed, except as disclosed in Note 3 to the unaudited condensed consolidated financial statements contained herein.

Recent Accounting Pronouncements

See Note 3 to our unaudited condensed consolidated financial statements for recent accounting pronouncements.

Item 3. Quantitative and Qualitative Disclosures About Market Risk.

Interest Rate Fluctuation Risk

We are exposed to market risk related to changes in interest rates. We invest a portion of our cash in investment-grade, interest-bearing securities. The primary objectives of our investment activities are to preserve principal, maintain liquidity and maximize total return. In order to achieve these objectives, we invest in money market funds, U.S. government and agency securities, corporate bonds and commercial paper in accordance with our investment policy. Our investment policy defines allowable investments and establishes guidelines relating to credit quality, diversification, and maturities of our investments to preserve principal and maintain liquidity. All investment securities have a credit rating of at least A-2/P-2/F2 from at least two National Recognized Statistical Rating Organizations. We do not have any direct investments in asset-backed securities, collateralized debt or loan obligations, or structured investment vehicles. Our primary exposure to market risk is interest income sensitivity, which is affected by changes in the general level of U.S. interest rates. Based on our $312.0 million of investments in money market funds, U.S. treasury notes, corporate bonds and municipal obligations as of September 30, 2023, an immediate 10% change in market interest rates would not have a material impact on the fair market value of our investment portfolio or on our financial position or results of operations.

As of September 30, 2023, we had $200.0 million in borrowings outstanding. The Term Loans bear interest at a per annum rate equal to, at our option, (i) a base rate plus a specified margin ranging from 2.50% to 3.00%, based on our senior secured net leverage ratio (as defined in the TLA Credit Agreement) or (ii) Term SOFR plus a credit spread adjustment of 0.10% plus a specified margin ranging from 3.50% to 4.00%, based on our senior secured net leverage ratio.. Based on the $200.0 million of principal outstanding as of September

36

30, 2023, an immediate 10% change in the SOFR would not have a material impact on our debt-related obligations, financial position or results of operations.

Foreign Currency Fluctuation Risk

We are not currently exposed to significant market risk related to changes in foreign currency exchange rates; however, we have contracted with and may continue to contract with foreign vendors that are located in Europe. Our operations may be subject to fluctuations in foreign currency exchange rates in the future.

Inflation Fluctuation Risk

Inflation generally affects us by increasing our cost of labor and clinical trial costs. We do not believe that inflation had a material effect on our business, financial condition or results of operations for each of the three and nine months ended September 30, 2023 and 2022.

Item 4. Controls and Procedures

Evaluation of Disclosure Controls and Procedures

Our management, including our principal executive officer and our principal financial officer, has evaluated the effectiveness of our disclosure controls and procedures, as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act, as of September 30, 2023. Based on that evaluation, our principal executive officer and principal financial officer concluded that, as of September 30, 2023, our disclosure controls and procedures were effective to provide reasonable assurance that the information we are required to disclose in reports that we file or submit under the Exchange Act is recorded, processed, summarized, and reported within the time periods specified in SEC rules and forms, and that such information is accumulated and communicated to our management, including our principal executive officer and principal financial officer, as appropriate, to allow timely decisions regarding required disclosure.

Changes in Internal Control over Financial Reporting

There were no changes in our internal control over financial reporting during the quarter ended September 30, 2023, that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

Limitations on Effectiveness of Controls and Procedures

Our management does not expect that our disclosure controls and procedures or our internal control over financial reporting will prevent all errors and all fraud. A control system, no matter how well designed and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefits of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, within our Company have been detected.

PART II. OTHER INFORMATION

Item 1. Legal Proceedings.

From time to time, we may become involved in litigation relating to claims arising from the ordinary course of business. Our management believes that there are currently no claims or actions pending against us, the ultimate disposition of which could have a material adverse effect on our results of operations or financial condition.

37

Item 1A. Risk Factors.

In addition to the other information included in this report, you should carefully consider the discussion of risk factors affecting the Company as set forth in Part I, Item 1A "Risk Factors” included in our Annual Report on Form 10-K for the year ended December 31, 2022, which could materially affect our business, financial condition or future results. The risks described in these reports are not the only risks facing the Company. Additional risks and uncertainties not currently known to us or that we currently deem to be immaterial may also materially adversely affect our business, financial condition, and operating results.

Item 2. Unregistered Sales of Equity Securities, Use of Proceeds, and Issuer Purchases of Equity Securities.

Purchases of Equity Securities

The following table summarizes information about our purchases of shares of our common stock for each of the months during the three months ended September 30, 2023.

Maxmium Approximate

Total Number of Shares

Dollar Value

Weighted Average

Shares of Common

of Shares of

Total Number of

Price Paid

Stock Purchases

Common Stock that May

Shares of Common

per Share of

as Part of Pubilicly

Yet to be Purchased

Period

    

Stock Purchased

    

Common Stock (1)

    

Announced Program (2)

    

under the Program (3)

July 1, 2023 through July 31, 2023

 

$

$

125,000

August 1, 2023 through August 31, 2023

 

764,800

$

32.81

764,800

$

99,910

September 1, 2023 through September 30, 2023

 

674,992

$

36.90

674,992

$

75,000

Total

1,439,792

$

34.73

1,439,792

$

75,000

(1)The weighted average price paid per share of common stock excludes commissions and transaction fees.
(2)On August 1, 2023, our Board of Directors approved a program providing for the repurchase of shares of common stock in an aggregate amount of up to $125.0 million, excluding commissions and transaction fees. The repurchase program may be suspended, terminated or modified at any time for any reason. Such repurchases may be pursuant to Rule 10b-18 or Rule 10b5-1 agreements as determined by our management and in accordance with the requirements of the Securities and Exchange Commission. All repurchased shares of common stock shown in the table above were retired.
(3)The dollar amount shown (in thousands), represents, as of the end of each period, the approximate dollar value of shares of common stock that may yet to be purchased under our publicly announced share repurchase program, exclusive of any commissions and transaction fees. The share repurchase program does not obligate us to repurchase any minimum dollar amount or number of shares of common stock.

Item 3. Defaults upon Senior Securities.

None.

38

Item 4. Mine Safety Disclosures.

Not applicable.

Item 5. Other Information.

During the three months ended September 30, 2023, no director or officer of the Company adopted or terminated a “Rule 10b5-1 trading arrangement” or “non-Rule 10b5-1 trading arrangement,” as each term is defined in Item 408(a) of Regulation S-K.

Item 6. Exhibits.

Exhibit

Incorporated by Reference

No.

    

Exhibit Description

    

Form

    

Date

   

Number

2.1+

Agreement and Plan of Merger, dated August 14, 2023, by and among Harmony Biosciences Holdings, Inc., Xylophone Acquisition Corp. and Zynerba Pharmaceuticals, Inc.

8-K/A

September 14, 2023

2.1

3.1

Amended and Restated Certificate of Incorporation of Harmony Biosciences Holdings, Inc.

8-K

August 21, 2020

3.1

3.2

Amended and Restated Bylaws.

8-K

August 21, 2020

3.2

10.1

Restricted Stock Unit Award Agreement dated October 4, 2023 with Sandip Kapadia

8-K

October 5, 2023

10.1

10.2

Restricted Stock Unit Award Agreement dated October 4, 2023 with Jeffrey Dierks

8-K

October 5, 2023

10.2

10.3

Credit Agreement, dated as of July 26, 2023, by an among JPMorgan Chase Bank, N.A., as administrative agent, and the lenders from time to time party thereto.

8-K

July 27, 2023

10.1

10.4

Guaranty, dated July 26, 2023, by and among each of the subsidiaries of Harmony Biosciences Holdings, Inc. and JPMorgan Chase Bank, N.A., as administrative agent.

8-K

July 27, 2023

10.2

10.5

Pledge and Security Agreement, dated July 26, 2023, by and among Harmony Biosciences Holdings, Inc. and each of the subsidiaries of Harmony Biosciences Holdings, Inc., and JPMorgan Chase Bank, N.A., as administrative agent.

8-K

July 27, 2023

10.3

10.6

First Incremental Amendment dated September 21, 2023 by and among Harmony Biosciences Holdings, Inc., JPMorgan Chase Bank, N.A., as administrative agent, and Bank of America, N.A., as incremental lender.

8-K

September 25, 2023

10.1

31.1*

Certification of Chief Executive Officer pursuant to Rules 13a-14(a) and 15d-14(a) of the Securities Exchange Act of 1934, as amended, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

31.2*

Certification of Chief Financial Officer pursuant to Rules 13a-14(a) and 15d-14(a) of the Securities Exchange Act of 1934, as amended, as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.

32.1**

Certification of Chief Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

32.2**

Certification of Chief Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.

101*

The following financial statements from the Companys Quarterly Report on Form 10-Q for the fiscal quarter ended September 30, 2023 formatted in Inline XBRL: (i) Balance Sheets, (ii) Statements of Operations, (iii) Statements of Stockholders Equity and (vi) Notes to Financial Statements, tagged as blocks of text and including detailed tags.

104*

Cover Page Interactive Date File (formatted as Inline XBRL and contained in Exhibit 101)

*

Filed herewith.

39

**

Furnished herewith. This certification is deemed furnished, and not filed, with the Securities and Exchange Commission and is not to be incorporated by reference into any filing of Harmony Biosciences Holdings, Inc. under the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, as amended, whether made before or after the date of this Quarterly Report on Form 10-Q, irrespective of any general incorporation language contained in such filing.

+

Schedules have been omitted pursuant to Item 601(b)(2) of Regulation S-K. The Company hereby undertakes to furnish supplemental copies of any of the omitted schedules upon request by the SEC; provided, however, that the Company may request confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934 for any schedules so furnished.

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

HARMONY BIOSCIENCES HOLDINGS, INC.

By:

/s/ Jeffrey M. Dayno

Name:

 

Jeffrey M. Dayno

Title:

President, Chief Executive Officer and Director (principal executive officer)

Date:

 

October 31, 2023

By:

 

/s/ Sandip Kapadia

Name:

 

Sandip Kapadia

Title:

Chief Financial Officer and Chief Administrative Officer (principal financial officer)

Date:

 

October 31, 2023

40

Exhibit 31.1

Certification of Principal Executive Officer

I, Jeffrey M. Dayno, certify that:

1.

I have reviewed this Quarterly Report on Form 10-Q of Harmony Biosciences Holdings, Inc.;

2.

Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

3.

Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

4.

The registrant’s other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

(a)

Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;

(b)

Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

(c)

Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

(d)

Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and

5.

The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):

(a)

All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and

(b)

Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.

Date: October 31, 2023

By:

/s/ Jeffrey M. Dayno

Jeffrey M. Dayno

President, Chief Executive Officer and Director

(Principal Executive Officer)


Exhibit 31.2

Certification of Principal Financial Officer

I, Sandip Kapadia, certify that:

1.

I have reviewed this Quarterly Report on Form 10-Q of Harmony Biosciences Holdings, Inc.;

2.

Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;

3.

Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;

4.

The registrants other certifying officer(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:

(a)

Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;

(b)

Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;

(c)

Evaluated the effectiveness of the registrants disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and

(d)

Disclosed in this report any change in the registrants internal control over financial reporting that occurred during the registrants most recent fiscal quarter (the registrants fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrants internal control over financial reporting; and

5.

The registrants other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrants auditors and the audit committee of the registrants board of directors (or persons performing the equivalent functions):

(a)

All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrants ability to record, process, summarize and report financial information; and

(b)

Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrants internal control over financial reporting.

Date: October 31, 2023

By:

/s/ Sandip Kapadia

Sandip Kapadia

Chief Financial Officer and Chief Administrative Officer

(Principal Financial Officer and Principal Accounting Officer)


Exhibit 32.1

Certification of Principal Executive Officer

Pursuant To 18 U.S.C. Section 1350,

as Adopted Pursuant to

Section 906 of The Sarbanes-Oxley Act of 2002

In connection with the Quarterly Report on Form 10-Q of Harmony Biosciences Holdings, Inc. (the “Company”) for the quarter ended September 30, 2023, as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that to such officer’s knowledge:

(1)The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and

(2)The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

Date: October 31, 2023

By:

/s/ Jeffrey M. Dayno

Jeffrey M. Dayno

President, Chief Executive Officer and Director

(Principal Executive Officer)

A signed original of this written statement required by Section 906 has been provided to the Company and will be retained by the Company and furnished to the Securities and Exchange Commission or its staff upon request.

The foregoing certification is being furnished solely pursuant to 18 U.S.C. Section 1350 and is not being filed as a part of the Report or on a separate disclosure document.


Exhibit 32.2

Certification of Principal Financial Officer

Pursuant To 18 U.S.C. Section 1350,

as Adopted Pursuant to

Section 906 of The Sarbanes-Oxley Act of 2002

In connection with the Quarterly Report on Form 10-Q of Harmony Biosciences Holdings, Inc. (the “Company”) for the period ended September 30, 2023 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I certify, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002, that to such officer’s knowledge:

(1)

The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and

(2)

The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.

Date: October 31, 2023

By:

/s/ Sandip Kapadia

Sandip Kapadia

Chief Financial Officer and Chief Administrative Officer

(Principal Financial Officer and Principal Accounting Officer)

A signed original of this written statement required by Section 906 has been provided to the Company and will be retained by the Company and furnished to the Securities and Exchange Commission or its staff upon request.

The foregoing certification is being furnished solely pursuant to 18 U.S.C. Section 1350 and is not being filed as a part of the Report or on a separate disclosure document.


v3.23.3
Document and Entity Information - shares
9 Months Ended
Sep. 30, 2023
Oct. 27, 2023
Cover [Abstract]    
Document Type 10-Q  
Document Quarterly Report true  
Document Period End Date Sep. 30, 2023  
Document Transition Report false  
Entity File Number 001-39450  
Entity Registrant Name HARMONY BIOSCIENCES HOLDINGS, INC.  
Entity Incorporation, State or Country Code DE  
Entity Tax Identification Number 82-2279923  
Entity Address, Address Line One 630 W.  
Entity Address, Address Line Two Germantown Pike  
Entity Address, Address Line Three Suite 215  
Entity Address, City or Town Plymouth Meeting  
Entity Address, State or Province PA  
Entity Address, Postal Zip Code 19462  
City Area Code 484  
Local Phone Number 539-9800  
Title of 12(b) Security Common Stock, par value $0.00001 value per share  
Trading Symbol HRMY  
Security Exchange Name NASDAQ  
Entity Current Reporting Status Yes  
Entity Interactive Data Current Yes  
Entity Filer Category Large Accelerated Filer  
Entity Small Business false  
Entity Emerging Growth Company false  
Entity Shell Company false  
Entity Common Stock, Shares Outstanding   58,571,944
Entity Central Index Key 0001802665  
Current Fiscal Year End Date --12-31  
Document Fiscal Year Focus 2023  
Document Fiscal Period Focus Q3  
Amendment Flag false  
v3.23.3
UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
CURRENT ASSETS:    
Cash and cash equivalents $ 324,603 $ 243,784
Investments, short-term 46,071 79,331
Trade receivables, net 67,264 54,740
Inventory, net 5,087 4,297
Prepaid expenses 14,269 9,347
Other current assets 5,704 8,786
Total current assets 462,998 400,285
NONCURRENT ASSETS:    
Property and equipment, net 428 573
Restricted cash 250 750
Investments, long-term 67,700 22,568
Intangible assets, net 143,069 160,953
Deferred tax asset 100,485 85,943
Other noncurrent assets 2,836 2,798
Total noncurrent assets 314,768 273,585
TOTAL ASSETS 777,766 673,870
CURRENT LIABILITIES:    
Trade payables 6,539 3,786
Accrued compensation 10,322 11,532
Accrued expenses 72,761 59,942
Current portion of long-term debt 15,000 2,000
Other current liabilities 7,786 1,624
Total current liabilities 112,408 78,884
NONCURRENT LIABILITIES:    
Long-term debt, net 182,131 189,647
Other noncurrent liabilities 1,895 2,501
Total noncurrent liabilities 184,026 192,148
TOTAL LIABILITIES 296,434 271,032
COMMITMENTS AND CONTINGENCIES (Note 12)
STOCKHOLDERS' EQUITY:    
Common stock-$0.00001 par value; 500,000,000 shares authorized at September 30, 2023 and December 31, 2022, respectively; 58,571,944 shares and 59,615,731 issued and outstanding at September 30, 2023 and December 31, 2022, respectively 1 1
Additional paid in capital 651,731 675,118
Accumulated other comprehensive (loss) income (516) (151)
Accumulated deficit (169,884) (272,130)
TOTAL STOCKHOLDERS' EQUITY 481,332 402,838
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY $ 777,766 $ 673,870
v3.23.3
UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS (Parenthetical) - $ / shares
Sep. 30, 2023
Dec. 31, 2022
UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS    
Common stock, par value $ 0.00001 $ 0.00001
Common stock, shares authorized 500,000,000 500,000,000
Common stock, shares issued 58,571,944 59,615,731
Common stock, shares outstanding 58,571,944 59,615,731
v3.23.3
UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME        
Net product revenues $ 160,268 $ 117,206 $ 413,610 $ 309,547
Revenue from Contract with Customer, Product and Service [Extensible Enumeration] us-gaap:ProductMember us-gaap:ProductMember us-gaap:ProductMember us-gaap:ProductMember
Cost of product sold $ 32,296 $ 22,959 $ 78,084 $ 56,596
Cost, Product and Service [Extensible Enumeration] us-gaap:ProductMember us-gaap:ProductMember us-gaap:ProductMember us-gaap:ProductMember
Gross profit $ 127,972 $ 94,247 $ 335,526 $ 252,951
Operating expenses:        
Research and development 17,499 40,548 45,757 60,794
Sales and marketing 23,418 20,467 70,518 58,210
General and administrative 22,546 21,331 67,417 61,374
Total operating expenses 63,463 82,346 183,692 180,378
Operating income 64,509 11,901 151,834 72,573
Loss on debt extinguishment (9,766)   (9,766)  
Other (expense) income, net (5) 56 (34) 96
Interest expense, net (2,906) (3,990) (8,327) (12,086)
Income before income taxes 51,832 7,967 133,707 60,583
Income tax (expense) benefit (13,371) 79,976 (31,461) 72,376
Net income 38,461 87,943 102,246 132,959
Unrealized income (loss) on investments 6 (149) (365) (178)
Comprehensive income $ 38,467 $ 87,794 $ 101,881 $ 132,781
EARNINGS PER SHARE:        
Basic $ 0.64 $ 1.48 $ 1.71 $ 2.25
Diluted $ 0.63 $ 1.44 $ 1.68 $ 2.18
Weighted average number of shares of common stock - basic 59,863,102 59,234,720 59,856,941 59,070,063
Weighted average number of shares of common stock - diluted 60,681,676 61,207,625 60,892,992 60,921,482
v3.23.3
UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY - USD ($)
$ in Thousands
Common Stock
Additional paid-in capital
Accumulated other comprehensive (loss) income
Accumulated deficit
Total
Beginning balance at Dec. 31, 2021 $ 1 $ 640,104   $ (453,598) $ 186,507
Beginning balance, shares at Dec. 31, 2021 58,825,769        
Net income       132,959 132,959
Unrealized income (loss) on investments     $ (178)   (178)
Issuance of common stock   408     408
Issuance of common stock (in shares) 8,050        
Exercise of stock options   5,275     5,275
Exercise of stock options, Shares 470,589        
Stock-based compensation   18,913     18,913
Ending balance at Sep. 30, 2022 $ 1 664,700 (178) (320,639) 343,884
Ending balance, shares at Sep. 30, 2022 59,304,408        
Beginning balance at Jun. 30, 2022 $ 1 655,143 (29) (408,582) 246,533
Beginning balance, shares at Jun. 30, 2022 59,117,749        
Net income       87,943 87,943
Unrealized income (loss) on investments     (149)   (149)
Issuance of common stock   408     408
Issuance of common stock (in shares) 8,050        
Exercise of stock options   2,143     2,143
Exercise of stock options, Shares 178,609        
Stock-based compensation   7,006     7,006
Ending balance at Sep. 30, 2022 $ 1 664,700 (178) (320,639) 343,884
Ending balance, shares at Sep. 30, 2022 59,304,408        
Beginning balance at Dec. 31, 2022 $ 1 675,118 (151) (272,130) 402,838
Beginning balance, shares at Dec. 31, 2022 59,615,731        
Net income       102,246 102,246
Unrealized income (loss) on investments     (365)   (365)
Repurchase of common stock   (50,543)     (50,543)
Repurchase of common stock (in shares) (1,439,792)        
Exercise of options and restricted stock units   4,314     $ 4,314
Exercise of options and restricted stock units, Shares 396,005        
Exercise of stock options, Shares         367,376
Stock-based compensation   22,842     $ 22,842
Ending balance at Sep. 30, 2023 $ 1 651,731 (516) (169,884) 481,332
Ending balance, shares at Sep. 30, 2023 58,571,944        
Beginning balance at Jun. 30, 2023 $ 1 694,038 (522) (208,345) 485,172
Beginning balance, shares at Jun. 30, 2023 59,999,658        
Net income       38,461 38,461
Unrealized income (loss) on investments     6   6
Repurchase of common stock   (50,543)     (50,543)
Repurchase of common stock (in shares) (1,439,792)        
Exercise of stock options   245     245
Exercise of stock options, Shares 12,078        
Stock-based compensation   7,991     7,991
Ending balance at Sep. 30, 2023 $ 1 $ 651,731 $ (516) $ (169,884) $ 481,332
Ending balance, shares at Sep. 30, 2023 58,571,944        
v3.23.3
UNAUDITED CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS - USD ($)
$ in Thousands
9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
CASH FLOWS FROM OPERATING ACTIVITIES    
Net income $ 102,246 $ 132,959
Adjustments to reconcile net income to net cash used in operating activities:    
Depreciation 350 312
Intangible amortization 17,884 17,005
Stock-based and employee stock purchase compensation expense 22,842 18,913
Stock appreciation rights market adjustment (531) 321
Debt issuance costs amortization 2,089 1,241
Deferred taxes (14,542) (81,679)
Amortization of premiums and accretion of discounts on Investment securities (2,031)  
Loss on debt extinguishment 9,766  
Other non-cash expenses 1,258 1,042
Change in operating assets and liabilities:    
Trade receivables (12,524) (20,222)
Inventory (790) 532
Prepaid expenses and other assets (1,759) (4,704)
Trade payables 2,753 9,048
Accrued expenses and other current liabilities 15,714 43,171
Other non-current liabilities (3) (151)
Net cash provided by operating activities 142,722 117,788
CASH FLOWS FROM INVESTING ACTIVITIES:    
Purchase of investment securities (105,856) (55,637)
Proceeds from maturities and sales of investment securities 95,687 872
Purchase of property and equipment (205) (172)
Milestone payments   (40,000)
Net cash used in investing activities (10,374) (94,937)
CASH FLOWS FROM FINANCING ACTIVITIES:    
Proceeds from issuance of common stock   408
Proceeds from long term debt 200,000  
Debt issuance costs (2,997)  
Extinguishment of debt (196,500)  
Extinguishment of debt exit fees (5,846)  
Principal repayment of long term debt (1,000) (1,500)
Repurchase of common stock (50,000)  
Payments of employee withholding taxes related to stock-based awards (514)  
Proceeds from exercised options 4,828 5,275
Net cash (used in) provided by financing activities (52,029) 4,183
NET INCREASE IN CASH, CASH EQUIVALENTS, AND RESTRICTED CASH 80,319 27,034
CASH, CASH EQUIVALENTS, AND RESTRICTED CASH-Beginning of period 244,534 235,059
CASH, CASH EQUIVALENTS, AND RESTRICTED CASH-End of period 324,853 262,093
Supplemental Disclosure of Cash Flow Information:    
Cash paid during the year for interest 15,653 11,334
Cash paid during the year for taxes $ 36,543 $ 9,702
v3.23.3
Organization and Description of Business
9 Months Ended
Sep. 30, 2023
Organization and Description of Business  
Organization and Description of Business

1. ORGANIZATION AND DESCRIPTION OF BUSINESS

The Company

Harmony Biosciences Holdings, Inc., and its consolidated subsidiary (the “Company”) was founded in July 2017 as Harmony Biosciences II, LLC, a Delaware limited liability company. The Company converted to a Delaware corporation named Harmony Biosciences II, Inc. in September 2017 and, in February 2020, the Company changed its name to Harmony Biosciences Holdings, Inc. The Company’s operations are conducted in its wholly owned subsidiary, Harmony Biosciences, LLC (“Harmony”), which was formed in May 2017. The Company is a commercial-stage pharmaceutical company focused on developing and commercializing innovative therapies for patients living with rare neurological diseases as well as patients living with other neurological diseases who have unmet medical needs. The Company is headquartered in Plymouth Meeting, Pennsylvania.

v3.23.3
Liquidity and Capital Resources
9 Months Ended
Sep. 30, 2023
Liquidity And Capital Resources  
Liquidity and Capital Resources

2. LIQUIDITY AND CAPITAL RESOURCES

The unaudited condensed consolidated financial statements have been prepared as though the Company will continue as a going concern, which contemplates the realization of assets and satisfaction of liabilities in the normal course of business. The Company had an accumulated deficit of $169,884 and $272,130, as of September 30, 2023 and December 31, 2022, respectively. As of September 30, 2023, the Company had cash, cash equivalents and investments of $438,374.

The Company believes that its existing cash, cash equivalents and investments on hand as of September 30, 2023, as well as additional cash generated from operating and financing activities will meet its operational liquidity needs and fund its planned investing activities for the next twelve months from the date of issuance of these unaudited condensed consolidated financial statements.

v3.23.3
Summary of Significant Accounting Policies
9 Months Ended
Sep. 30, 2023
Summary of Significant Accounting Policies  
Summary of Significant Accounting Policies

3. SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of Presentation

The unaudited condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”) and include all adjustments necessary for the fair presentation of the Company’s financial position for the periods presented. All intercompany accounts and transactions have been eliminated in consolidation. The unaudited condensed consolidated balance sheet as of September 30, 2023, the unaudited condensed consolidated statements of cash flows for the three and nine months ended September 30, 2023, and 2022, and the unaudited condensed consolidated statements of operations and comprehensive income and the unaudited condensed consolidated statements of shareholders’ equity for the three and nine months ended September 30, 2023 and 2022, are unaudited. The balance sheet as of December 31, 2022, was derived from audited financial statements as of and for the year ended December 31, 2022. The unaudited interim condensed consolidated financial statements have been prepared on the same basis as the audited annual financial statements as of and for the year ended December 31, 2022, and, in the opinion of management, reflect all adjustments, which include only normal recurring adjustments, necessary for the fair presentation of the Company’s financial position as of September 30, 2023, and the results of its operations and its cash flows for the three and nine months ended September 30, 2023 and 2022. The unaudited condensed consolidated results of operations are not necessarily indicative of the results that may occur for the full fiscal year. Certain information and disclosures normally included in the financial statements prepared in accordance with GAAP have been condensed or omitted under the SEC’s rules and regulations. These unaudited condensed consolidated financial statements should be read

in conjunction with the audited financial statements and accompanying notes thereto contained in the Company’s Annual Report on Form 10-K for the year ended December 31, 2022.

Use of Estimates

The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts and disclosures in the unaudited condensed consolidated financial statements, including the notes thereto, and elsewhere in this report. Actual results may differ significantly from estimates, which include rebates due pursuant to commercial and government contracts, accrued research and development expenses, stock-based compensation expense and income taxes.

Cash, Cash Equivalents and Restricted Cash

Cash and cash equivalents and restricted cash consist of cash and, if applicable, highly liquid investments with an original maturity of three months or less when purchased, including investments in Money Market Funds and debt securities that approximate fair value. The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheet and the statements of cash flows.

    

As of

    

September 30, 

    

December 31, 

2023

2022

Cash and cash equivalents

$

324,603

$

243,784

Restricted cash

 

250

 

750

Total cash, cash equivalents, and restricted cash shown in the statements of cash flows

$

324,853

$

244,534

Restricted cash includes amounts required to be held as a security deposit in the form of letters of credit for the Company’s credit card program and the fleet program.

Investments

The Company’s investments consist of debt securities that are classified as available-for-sale. Short-term and long-term investments are carried at fair value and unrealized gains and losses are recorded as a component of accumulated comprehensive income in stockholders’ equity. The amortization of premiums and accretion of discounts adjust the carrying value of investments and are recorded in interest expense, net, on the unaudited condensed consolidated statements of operations and comprehensive income. Interest income and realized gains and losses, if any, are also recorded in interest expense, net, on the unaudited condensed consolidated statement of operations and comprehensive income. Realized gains and losses that result from the sale of investments are determined on a specific identification basis.

At each reporting period, the Company reviews any unrealized losses position to determine if the decline in the fair value of the underlying investments is a result of credit losses or other factors. If the assessment indicates that a credit loss exists, any impairment is recognized as an allowance for credit losses in our consolidated statement of operations.

Interest income generated from our investments and cash equivalents, which is included in interest expense, net, was $3,384 and $8,537 for the three and nine months ended September 30, 2023, respectively, compared to $828 and $1,145 for the three and nine months ended September 30, 2022, respectively.

Concentrations of Risk

Substantially all of the Company’s cash and money market funds are held in four financial institutions. Due to their size, the Company believes these financial institutions represent minimal credit risk. Deposits may

exceed the amount of insurance provided on such deposits by the Federal Deposit Insurance Corporation for U.S. institutions. The Company has not experienced any losses on its deposits of cash and cash equivalents. The Company believes that it is not exposed to significant credit risk due to the financial position of the depository institutions in which those deposits are held.

The Company is subject to credit risk from its trade receivables related to its product sales. The Company extends credit to specialty pharmaceutical distribution companies within the United States. Customer creditworthiness is monitored, and collateral is not required. Historically, the Company has not experienced credit losses on its accounts receivable. The Company monitors its exposure within accounts receivable and would record a reserve against uncollectible accounts receivable if necessary. As of September 30, 2023, three customers accounted for 100% of gross accounts receivable; Caremark LLC (“CVS Caremark”), which accounted for 37% of gross accounts receivable; Accredo Health Group, Inc. (“Accredo”), which accounted for 37% of gross accounts receivable; and PANTHERx Specialty Pharmacy LLC (“Pantherx”), which accounted for 26% of gross accounts receivable. As of December 31, 2022, three customers accounted for 100% of gross accounts receivable; CVS Caremark, which accounted for 41% of gross accounts receivable, Accredo, which accounted for 35% of gross accounts receivable; and Pantherx, which accounted for 24% of gross accounts receivable.

For the nine months ended September 30, 2023, three customers accounted for 100% of gross product revenues; CVS Caremark accounted for 37% of gross product revenues; Accredo accounted for 32% of gross product revenues; and Pantherx accounted for 31% of gross product revenues. For the nine months ended September 30, 2022, three customers accounted for 100% of gross product revenues; CVS Caremark accounted for 40% of gross product revenues; Pantherx accounted for 30% of gross product revenues; and Accredo accounted for 30% of gross product revenues.

The Company depends on a single source supplier for each of its product and active pharmaceutical ingredient.

Share Repurchases

The Company accounts for share repurchases as constructive retirements, whereby it reduces common stock and additional paid-in capital by the amount of the original issuance, with any excess purchase price recorded as a reduction to retained earnings. Under this method, issued and outstanding shares of common stock are reduced by the amount of shares of common stock repurchased, and no treasury stock is recognized on the condensed consolidated financial statements.

Recently Issued Accounting Pronouncements

The Company did not adopt any new accounting pronouncements that had a material effect on its condensed consolidated financial statements during the three and nine months ended September 30, 2023.

v3.23.3
Investments
9 Months Ended
Sep. 30, 2023
Investments  
Investments

4. INVESTMENTS

The carrying value and amortized cost of the Company’s available-for-sale debt securities, summarized by type of security, consisted of the following:

September 30, 2023

Amortized

Unrealized

Unrealized

Fair

Cost

Gains

Losses

Value

Short-term:

Commercial paper

$

27,717

1

(13)

$

27,705

Corporate debt securities

16,456

3

(7)

16,452

U.S. government securities

1,915

(1)

1,914

Total short-term investments

$

46,088

4

(21)

$

46,071

Long-term:

Commercial paper

$

1,623

(2)

$

1,621

Corporate debt securities

39,497

14

(155)

39,356

U.S. government securities

27,079

(356)

26,723

Total long-term investments

$

68,199

14

(513)

$

67,700

December 31, 2022

Amortized

Unrealized

Unrealized

Fair

Cost

Gains

Losses

Value

Short-term:

Commercial paper

$

26,553

15

(34)

$

26,534

Corporate debt securities

49,213

9

(73)

49,149

U.S. government securities

3,658

(10)

3,648

Total short-term investments

$

79,424

24

(117)

$

79,331

Long-term:

Commercial paper

$

853

1

$

854

Corporate debt securities

21,516

11

(68)

21,459

U.S. government securities

257

(2)

255

Total long-term investments

$

22,626

12

(70)

$

22,568

The Company classifies investments with an original maturity of less than one year as current and investments with an original maturity date of greater than one year as noncurrent on its unaudited condensed consolidated balance sheet. The investments classified as noncurrent have original maturity dates ranging from 1-2 years. The Company did not have any available-for-sale debt security investments in a continuous unrealized loss position of greater than 12 months as of September 30, 2023 and December 31, 2022, respectively.

v3.23.3
Fair Value Measurements
9 Months Ended
Sep. 30, 2023
Fair Value Measurements  
Fair Value Measurements

5. FAIR VALUE MEASUREMENTS

The Company’s unaudited condensed consolidated financial statements include cash, cash equivalents, restricted cash, accounts payable, and accrued liabilities, all of which are short term in nature and, accordingly, approximate fair value.

It is the Company’s policy to measure non-financial assets and liabilities at fair value on a nonrecurring basis. These non-financial assets and liabilities are not measured at fair value on an ongoing basis but are subject to fair value adjustments in certain circumstances (such as evidence of impairment), which, if material, are disclosed in the accompanying footnotes.

The Company measures certain assets and liabilities at fair value based on the fair value hierarchy that prioritizes inputs to valuation techniques used to measure fair value into three levels based on the source of inputs as follows:

Level 1—Valuations based on unadjusted quoted prices in active markets for identical assets or liabilities.

Level 2—Valuations based on observable inputs and quoted prices in active markets for similar assets and liabilities.

Level 3—Valuations based on unobservable inputs and models that are supported by little or no market activity.

Money market funds are classified as Level 1 fair value instruments. Investments in available-for-sale debt securities are classified as Level 2 and carried at fair value, which we estimate utilizing a third-party pricing service. The pricing service utilizes industry standard valuation models whereby all significant inputs, including benchmark yields, reported trades, broker/dealer quotes, issuer spreads, bids, offers, or other market-related data, are observable. We validate valuations obtained from third-party services by obtaining market values from other pricing sources. The Company did not classify any assets or liabilities as Level 3 as of September 30, 2023 or December 31, 2022.

The Company’s assets measured at fair value consisted of the following:

September 30, 2023

December 31, 2022

Total

Level 1

Level 2

Total

Level 1

Level 2

Assets

Cash equivalents

$

198,135

198,135

$

184,977

184,977

Commercial paper

29,326

29,326

27,388

27,388

Corporate debt securities

55,808

55,808

70,608

70,608

U.S. government securities

28,637

28,637

3,903

3,903

Total

$

311,906

198,135

113,771

$

286,876

184,977

101,899

v3.23.3
Inventory
9 Months Ended
Sep. 30, 2023
Inventory  
Inventory

6. INVENTORY

Inventory, net consisted of the following:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Raw materials

$

932

$

838

Work in process

 

1,833

 

1,513

Finished goods

 

2,611

 

2,565

Inventory, gross

 

5,376

 

4,916

Reserve for excess inventory

 

(289)

 

(619)

Total inventory, net

$

5,087

$

4,297

v3.23.3
Intangible Assets
9 Months Ended
Sep. 30, 2023
Intangible Assets  
Intangible Assets

7. INTANGIBLE ASSETS

In August 2019, the Company received FDA approval of WAKIX® (pitolisant) for the treatment of excessive daytime sleepiness (“EDS”) in adult patients with narcolepsy. This event triggered a milestone payment of $75,000 under the provisions of the 2017 LCA (defined below) which the Company capitalized as an intangible asset. The Company determined a useful life of 10 years for such intangible asset, and, as of September 30, 2023, the remaining useful life was 6.0 years.

In October 2020, the Company received FDA approval for the New Drug Application (“NDA”) for WAKIX for the treatment of cataplexy in adult patients with narcolepsy. This event triggered a milestone payment of $100,000 under the provisions of the 2017 LCA which the Company capitalized as an intangible asset and paid in January of 2021. The Company determined a useful life of 9 years for such intangible asset, and, as of September 30, 2023, the remaining useful life was 6.0 years.

In February 2022, the Company attained $500,000 in life-to-date aggregate net sales of WAKIX in the United States. This event triggered a final $40,000 payment under the provisions of the 2017 LCA which the Company capitalized as an intangible asset and paid in March of 2022. The Company determined a useful life of 7.6 years for such intangible asset, and, as of September 30, 2023, the remaining useful life was 6.0 years.

Amortization expense was $5,962 and $5,961 for the three months ended September 30, 2023 and 2022, respectively, and $17,884 and $17,005 for the nine months ended September 30, 2023 and 2022, respectively, and is recorded in general and administrative expenses on the unaudited condensed consolidated statements of operations and comprehensive income.

The Company expects the future annual amortization expense for the unamortized intangible assets to be as follows:

Years ending December 31, 

    

2023 (Excluding the nine months ended September 30, 2023)

$

5,961

2024

 

23,845

2025

 

23,845

2026

 

23,845

2027

 

23,845

Thereafter

41,728

Total

$

143,069

The gross carrying amount and net book value of the intangible asset is as follows:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Gross Carrying Amount

$

215,000

$

215,000

Accumulated Amortization

 

(71,931)

 

(54,047)

Net Book Value

$

143,069

$

160,953

v3.23.3
License Agreements and Asset Purchase Agreements
9 Months Ended
Sep. 30, 2023
License Agreements and Asset Purchase Agreements  
License Agreements and Asset Purchase Agreements

8. LICENSE AGREEMENTS AND ASSET PURCHASE AGREEMENTS

License Agreements

In July 2017, Harmony entered into a License Agreement (the “2017 LCA”) with Bioprojet Société Civile de Recherche (“Bioprojet”) whereby Harmony acquired the exclusive right to commercialize the pharmaceutical compound pitolisant for the treatment, and/or prevention, of narcolepsy, obstructive sleep apnea, idiopathic hypersomnia, and Parkinson’s disease as well as any other indications unanimously agreed by the parties in the United States and its territories. A milestone payment of $50,000 was due upon acceptance by the FDA of

pitolisant’s NDA, which was achieved in February 2019 and was expensed within research and development for the year ended December 31, 2019. A milestone payment of $77,000, which included a $2,000 fee that is described below, was due upon FDA approval of WAKIX (pitolisant) for treatment of EDS in adult patients with narcolepsy, which was achieved in August 2019. The $2,000 payment and $75,000 milestone payment were paid in August and November 2019, respectively. In addition, a milestone payment of $102,000, which included a $2,000 fee was due upon the FDA approval of the NDA for WAKIX for the treatment of cataplexy in adult patients with narcolepsy. The $2,000 payment was paid in October 2020 and a $100,000 milestone payment was paid in January 2021. A final $40,000 milestone payment was paid to Bioprojet in March 2022 upon WAKIX attaining $500,000 in aggregate net sales in the United States. The 2017 LCA also requires a fixed trademark royalty and a tiered royalty based on net sales, which is payable to Bioprojet on a quarterly basis. The Company incurred $29,665 and $20,944 for the three months ended September 30, 2023 and 2022, respectively, and $71,267 and $51,741 for the nine months ended September 30, 2023 and 2022, respectively, for sales-based, trademark and tiered royalties recognized as cost of product sold. As of September 30, 2023 and December 31, 2022, the Company had accrued $29,665 and $25,367, respectively, for sales-based, trademark and tiered royalties.  

On July 31, 2022, Harmony entered into a License and Commercialization Agreement (the “2022 LCA”) with Bioprojet whereby Harmony obtained exclusive rights to manufacture, use and commercialize one or more new products based on pitolisant in the United States and Latin America, with the potential to add additional indications and formulations upon agreement of both parties. Harmony paid an initial, non-refundable $30,000 licensing fee in October 2022 and additional payments of up to $155,000 are potentially due under the 2022 LCA upon the achievement of certain future development and sales-based milestones. In addition, there are other payments due upon achievement of development milestones for new indications and formulations as agreed upon by both parties. The 2022 LCA also requires a fixed trademark royalty and a tiered royalty based on net sales upon commercialization, which will be payable to Bioprojet on a quarterly basis.

Agreement Related to Intellectual Property

In August 2021, the Company entered into an asset purchase agreement with ConSynance Therapeutics, Inc. (the “APA”) to acquire HBS-102 (formerly referred to as “CSTI-100”), a potential first-in-class molecule with a novel mechanism of action. Under the terms of the APA, the Company acquired full development and commercialization rights globally, with the exception of Greater China, for $3,500. The Company accounted for the transaction as an asset acquisition as substantially all of the fair value of the assets acquired was concentrated in a single identified asset. In March 2023, the Company achieved a preclinical milestone, which triggered a $750 payment under the provisions of the APA, which the Company recognized as an IPR&D charge recorded in research and development within the unaudited condensed consolidated statement of operations and comprehensive income for the nine months ended September 30, 2023. There are additional payments due under the APA upon the achievement of certain milestones including $1,000 for preclinical milestones, $19,000 for development milestones, $44,000 for regulatory milestones and $110,000 for sales milestones.

v3.23.3
Accrued Expenses
9 Months Ended
Sep. 30, 2023
Accrued Expenses  
Accrued Expenses

9. ACCRUED EXPENSES

Accrued expenses consist of the following:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Royalties due to Bioprojet

$

29,665

$

25,367

Rebates and other sales deductions

 

31,853

 

27,860

Interest

3,140

3,286

Selling and marketing

 

2,253

 

1,135

Research and development

 

2,190

 

358

Professional fees, consulting, and other services

 

1,841

 

1,163

Other expenses

 

1,819

 

773

$

72,761

$

59,942

v3.23.3
Debt
9 Months Ended
Sep. 30, 2023
Debt  
Debt

10. DEBT

Term Loan A Credit Agreement

On July 26, 2023, the Company entered into a Credit Agreement (the “TLA Credit Agreement”) with JPMorgan Chase Bank, N.A., as “Administrative Agent”, and certain lenders. The TLA Credit Agreement provides for a five-year senior secured term loan (the “TLA Term Loan”) in an aggregate principal amount of $185,000.

On September 21, 2023, the Company entered into the First Incremental Amendment (the “First Incremental Amendment”) with the Administrative Agent and Bank of America, N.A., as incremental lender. The First Incremental Amendment provides for an incremental senior secured term loan (the “Incremental Term Loan”) in an aggregate principal amount of $15,000. The First Incremental Amendment amends the TLA Credit Agreement and provides that the Incremental Term Loan will have identical terms as the TLA Term Loan.

The repayment schedule for both the TLA Term Loan and the Incremental Term Loan (together, the “Term Loans”) consists of quarterly $3,750 principal payments, which commence on December 31, 2023, increasing to quarterly $5,000 principal payments beginning on December 31, 2025, with a $115,000 payment due on the maturity date of July 26, 2028. The Term Loans bear interest at a per annum rate equal to, at the Company’s option, (i) a base rate plus a specified margin ranging from 2.50% to 3.00%, based on the Company’s senior secured net leverage ratio (as defined in the TLA Credit Agreement) or (ii) Term SOFR plus a credit spread adjustment of 0.10% plus a specified margin ranging from 3.50% to 4.00%, based on the Company’s senior secured net leverage ratio.

The net cash received related to the Term Loans as a result of the transactions, less debt issuance costs of $2,997, was $197,003. The debt issuance costs related to the Term Loans will be amortized as additional interest expense over the loan term of the TLA Credit Agreement. The fair value of the Term Loans as of September 30, 2023 was $199,820.

Blackstone Credit Agreement

In August 2021, the Company entered into the Blackstone Credit Agreement that provided for (i) a senior secured term loan facility in an aggregate original principal amount of $200,000 (the “Initial Term Loan”) and (ii) a senior secured delayed draw term loan facility in an aggregate principal amount up to $100,000 (the “DDTL”). The DDTL was initially available to draw down through August 9, 2022. In August 2022, the Company entered into an agreement to extend the expiration date of the DDTL to August 9, 2023, for which the Company would pay a ticking fee at a rate of 1% per annum on the undrawn portion of the DDTL (the “Ticking Fee”), which commenced on August 10, 2022.

Net cash received from the Initial Term Loan was $191,849, net of debt issuance costs of $8,151. In addition, the Company paid $1,000 in debt issuance costs relating to the DDTL, which was initially recorded in other current assets within the unaudited condensed consolidated balance sheet.

In connection with the TLA Credit Agreement, the Company extinguished the Blackstone Credit Agreement, which required a payoff amount of $207,308 consisting of principal repayment, interest, exit fees, Ticking Fee and a prepayment premium. The Company recognized a loss on extinguishment of debt of $9,766 relating to the Blackstone Credit Agreement within the Company’s unaudited condensed consolidated statements of operation and comprehensive income for the three and nine months ended September 30, 2023. In addition, the Company recognized $1,972 relating to unamortized debt issuance costs relating to the DDTL and the Ticking Fee, which was recorded in interest expense, net within the unaudited condensed consolidated statement of operations and comprehensive income for the three and nine months ended September 30, 2023.

Long-term debt, net consists of the following:

    

September 30, 

    

December 31, 

2023

2022

Liability component - principal

$

200,000

$

197,500

Unamortized debt discount associated with debt financing costs

 

(2,869)

 

(5,853)

Liability component - net carrying value

197,131

191,647

Less current portion

(15,000)

(2,000)

Long-term debt, net

$

182,131

$

189,647

Future minimum payments relating to long-term debt, net as of September 30, 2023, for the periods indicated below consists of the following:

Years ending December 31, 

2023 (Excluding the nine months ended September 30, 2023)

$

3,750

2024

 

15,000

2025

 

16,250

2026

 

20,000

2027

 

20,000

Thereafter

125,000

Total

$

200,000

Interest expense related to the Company’s long-term debt, net, is included in interest expense, net in the unaudited condensed consolidated statements of operations and comprehensive income and consists of the following:

Three Months Ended

Nine Months Ended

September 30, 

September 30, 

2023

    

2022

2023

    

2022

Interest on principal balance

$

4,791

$

4,513

$

15,900

$

12,110

Amortization of deferred financing costs

 

2,221

 

418

 

3,061

 

1,241

Total term loan interest expense

$

7,012

$

4,931

$

18,961

$

13,351

v3.23.3
Leases
9 Months Ended
Sep. 30, 2023
Leases  
Leases

11. LEASES

In June 2018, the Company entered into an operating lease for approximately fifteen thousand square feet of office space in Plymouth Meeting, PA, which expires in May 2024. The Company subsequently entered into two separate operating leases for additional office space in Plymouth Meeting, PA, which include approximately thirteen thousand square feet and seven thousand square feet of additional office space, respectively, and expire in May 2024. The terms of the lease payments provide for rental payments on a monthly basis and on a graduated scale. The Company also leases a fleet of automobiles that are used by its sales representatives and are classified as operating leases.

Operating lease right-of-use assets and operating lease liabilities are recognized based on the present value of the future lease payments using our incremental borrowing rate. Leases with an initial term of 12 months or less are not recorded on the balance sheet. Our leases have remaining lease terms of less than 1 year to 3 years, some of which may include the option to extend or terminate the leases.

The Company recorded operating lease costs of $473 and $378 for the three months ended September 30, 2023 and 2022, respectively, and $1,295 and $1,155 for the nine months ended September 30, 2023 and 2022, respectively.

As of September 30, 2023, the weighted-average remaining lease term for operating leases was 1.8 years and the weighted-average discount rate for operating leases was 6.0%.

Supplemental balance sheet information related to operating leases was as follows:

Leases

Classification

September 30, 2023

  

December 31, 2022

Assets

Operating lease right-of-use assets

Other noncurrent assets

$

2,456

$

2,312

Liabilities

Operating lease liability, current portion

Other current liabilities

$

1,683

$

1,614

Operating lease liability, long-term

Other long-term liabilities

901

975

Total operating lease liabilities

$

2,584

$

2,589

Supplemental cash flow information related to operating leases was as follows:

September 30, 2023

September 30, 2022

Operating cash flows from operating leases

$

1,448

$

1,297

Right of use assets obtained in exchange for operating lease obligations

$

1,592

$

485

Future payments under noncancelable operating leases with initial terms of one year or more as of September 30, 2023 consisted of the following:

Years ending December 31, 

    

2023 (Excluding the nine months ended September 30, 2023)

$

558

2024

 

1,407

2025

 

532

2026

 

252

2027

 

Thereafter

 

Total lease payments

2,749

Less: imputed interest

(165)

Total lease liabilities

$

2,584

v3.23.3
Commitments and Contingencies
9 Months Ended
Sep. 30, 2023
Commitments and Contingencies.  
Commitments and Contingencies

12. COMMITMENTS AND CONTINGENCIES

Litigation

From time to time, the Company is subject to claims and suits arising in the ordinary course of business. The Company accrues such liabilities when they are known, if they are deemed probable and can be reasonably estimated. As of September 30, 2023, there were no material claims or suits outstanding.

v3.23.3
Stockholders' Equity
9 Months Ended
Sep. 30, 2023
Stockholders' Equity  
Stockholders' Equity

13. STOCKHOLDERS’ EQUITY

Common Stock

The holders of common stock are entitled to one vote for each share held on all matters submitted to a vote of the Company’s stockholders. The holders of common stock do not have any cumulative voting rights. Holders of common stock are entitled to receive ratably any dividends declared by the Company’s board of directors out of funds legally available for that purpose, subject to any preferential dividend rights of any outstanding preferred stock. The Company’s common stock has no preemptive rights, conversion rights or other subscription rights or redemption or sinking fund provisions.

Share Repurchase Program

On August 1, 2023, the Company’s Board of Directors approved a program providing for the repurchase of shares of common stock in an aggregate amount of up to $125,000, excluding commissions and transaction fees (the “August 2023 Repurchase Program”). The August 2023 Repurchase Program may be suspended, terminated or modified at any time for any reason. During the three and nine months ended September 30, 2023, the Company repurchased and cancelled 1,439,792 shares of common stock at an aggregate cost of $50,000, exclusive of commissions and transaction fees. As of September 30, 2023 the remaining amount of common stock authorized for repurchases was $75,000.

See Note 18 to our unaudited condensed consolidated financial statements for information related to the termination of the August 2023 Repurchase Program as of October 27, 2023.

v3.23.3
Stock Incentive Plan and Stock-based Compensation
9 Months Ended
Sep. 30, 2023
Stock Incentive Plan and Stock-based Compensation  
Stock Incentive Plan and Stock-based Compensation

14. STOCK INCENTIVE PLAN AND STOCK-BASED COMPENSATION

2020 Stock Incentive Plan

In connection with the Company’s IPO, the board of directors adopted, and its stockholders approved, the 2020 Incentive Award Plan (the “2020 Plan”), in order to facilitate the grant of cash and equity incentives to directors, employees (including the Company’s named executive officers) and consultants of the Company and its subsidiaries. The 2020 Plan provides for the grant of stock options, including incentive stock options (“ISOs”) and non-qualified stock options (“NSOs”), SARs, restricted stock, dividend equivalents, restricted stock units (“RSUs”) and other stock or cash-based awards.

Stock options and stock appreciation rights under the 2020 Plan have a 10-year contractual term and vest over the vesting period specified in the applicable award agreement, at achievement of a performance requirement, or upon change of control (as defined in the applicable plan). RSUs vest over the vesting period specified in the applicable award agreement, at achievement of a performance requirement, or upon change of control (as defined in the applicable plan). As of September 30, 2023, there were 6,755,091 shares of common stock available for issuance under the 2020 Plan. The number of shares that may be issued under the 2020 Plan will automatically increase on January 1 of each year in an amount equal to the lesser of (i) 4.0% of the shares of the Company’s common stock outstanding on December 31 of the preceding year or (ii) an amount determined by the Company’s board of directors.

2017 Stock Incentive Plan

In August 2017, the Company adopted an equity incentive plan (the “2017 Plan”). Under the 2017 Plan, directors, officers, employees, consultants, and advisors of the Company can be paid incentive compensation measured by the value of the Company’s shares of common stock through grants of stock options, stock appreciation rights (“SARs”), or restricted stock. Following the adoption of the 2020 Plan, no further grants have been, or will be, made under the 2017 Plan. However, the 2017 Plan will continue to govern the terms and conditions of outstanding awards granted under it.

Stock Options

The following table summarizes stock option activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Exercise

Contractual

    

Awards

    

Price

    

Term

Awards outstanding—December 31, 2022

 

6,460,947

$

30.90

 

7.86

Awards issued

 

376,422

$

36.71

 

  

Awards exercised

 

(367,376)

$

12.02

 

  

Awards forfeited

 

(206,318)

$

24.84

 

  

Awards outstanding—September 30, 2023

 

6,263,675

$

32.55

 

7.39

Stock Appreciation Rights

The following table summarizes SARs activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Exercise

Contractual

    

Awards

    

Price

    

Term

Awards outstanding—December 31, 2022

 

43,208

$

9.38

 

6.32

Awards issued

 

$

 

  

Awards exercised

 

$

 

  

Awards forfeited

 

$

 

  

Awards outstanding—September 30, 2023

 

43,208

$

9.38

 

5.58

Restricted Stock Units

The following table summarizes RSU activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Grant Date

Contractual

    

Awards

    

Fair Value

    

Term

Awards outstanding—December 31, 2022

 

60,000

$

29.03

 

8.24

Awards issued

 

$

 

  

Awards vested

 

(30,000)

$

29.03

 

  

Awards forfeited

 

$

 

  

Awards outstanding—September 30, 2023

 

30,000

$

29.03

 

7.49

As of September 30, 2023 and December 31, 2022, stock awards issued under the 2017 and 2020 Plans of 3,141,836 and 1,818,045 shares of common stock, respectively, were vested.

Value of Stock Options and SARs

The Company values options and SARs using the Black-Scholes option-pricing model. The Company lacks sufficient historical company-specific volatility information. Therefore, the Company estimates expected stock volatility based on historical volatility of peer companies and expects to continue to do so until such time as it has adequate historical data regarding the volatility of its own traded stock price. For options with service-

based vesting conditions, the expected term of the Company’s stock options has been determined utilizing the “simplified” method for awards that qualify as “plain-vanilla” options. For SARs, the expected term is based upon the weighting of certain future events. The risk-free interest rate is determined by reference to the U.S. Treasury yield curve in effect at the time of grant of the award for the time periods approximately equal to the expected term of the award. An expected dividend yield of 0% is based on the fact that the Company has never paid cash dividends and does not expect to do so in the foreseeable future.

The assumptions used to value the awards are summarized in the following table.

As of

    

September 30, 

    

December 31, 

    

2023

    

2022

Dividend yield

 

0.00

%  

0.00

%

Expected volatility

 

76.32 - 80.21

%  

72.57 - 77.08

%

Risk-free interest rate

 

3.42 - 4.61

%  

1.99 - 4.05

%

Lack of marketability discount

 

0.00

%  

0.00

%

Expected term (years)

 

2.4 - 6.3

 

3.1 - 6.3

Value of RSUs

The fair value of RSUs is equal to the value of the Company’s common stock on the grant date.

The weighted average per share fair value of awards issued under the 2017 Plan and 2020 Plan was $20.13 and $18.88 on September 30, 2023 and December 31, 2022, respectively.

Stock-Based Compensation Expense

Stock-based compensation expense, net for the three and nine months ended September 30, 2023 and 2022, was recorded in the unaudited condensed consolidated statements of operations and comprehensive income in the following line items:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

    

2023

    

2022

    

2023

    

2022

Research and development expense

$

1,030

$

522

$

2,962

$

1,866

Sales and marketing expense

 

1,218

 

1,096

 

3,437

 

2,956

General and administrative expense

 

5,709

 

5,349

 

15,912

 

14,412

$

7,957

$

6,967

$

22,311

$

19,234

Stock-based compensation expense, net related to options and RSUs issued under the 2017 Plan and 2020 Plan is included in stockholder’s equity, and a liability for SARs is included in other non-current liabilities, in the Company’s unaudited condensed consolidated balance sheet. As of September 30, 2023, the total unrecognized stock-based compensation expense related to options and RSUs was $67,842. Such amount will be recognized in the Company’s consolidated statement of operations over a weighted average period of 2.4 years.

Employee Stock Purchase Plan

The 2020 Employee Stock Purchase Plan (“ESPP”) was adopted by the Company’s Board of Directors on April 30, 2021. The ESPP permits eligible employees to purchase shares of the Company’s common stock at a 15% discount from the lesser of the fair market value per share of the Company’s common stock on the first day of the offering period or the fair market value of the Company’s common stock on the purchase date. Funds are collected from employees through after-tax payroll deductions. The total number of shares reserved for issuance under the ESPP was initially 629,805, which will automatically increase on January 1 of each year in an amount equal to the lesser of (i) 1.0% of the shares of the Company’s common stock outstanding on

December 31 of the preceding year or (ii) an amount determined by the Company’s board of directors. It is intended that the ESPP meet the requirements for an “employee stock purchase plan” under Section 423 of the Internal Revenue Code. There were no shares issued under the ESPP for the three months ended September 30, 2023 and 2022, and there were 14,043 and 14,889 shares issued under the ESPP for the nine months ended September 30, 2023 and 2022, respectively. The discount on the ESPP was $100 and $86 for the three months ended September 30, 2023 and 2022, respectively, and $308 and $271 for the nine months ended September 30, 2023 and 2022, respectively, and is recorded within stock-based compensation expense.

v3.23.3
Earnings per Share
9 Months Ended
Sep. 30, 2023
Earnings per Share  
Earnings per Share

15. EARNINGS PER SHARE

Basic earnings per share is calculated by dividing net income by the weighted average number of shares of common stock outstanding. Diluted net income per share of common is computed under the treasury stock method by using the weighted average number of shares of common stock outstanding, plus, for periods with net income, the potential dilutive effects of stock options, stock appreciation rights and restricted stock units.

The following table sets forth the computation of basic and diluted net income per share:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Numerator

 

  

 

  

  

 

  

Net income

$

38,461

$

87,943

$

102,246

$

132,959

Denominator

 

  

 

  

 

  

 

  

Net income per share of common stock - basic

$

0.64

$

1.48

$

1.71

$

2.25

Net income per share of common stock- diluted

$

0.63

$

1.44

$

1.68

$

2.18

Weighted average number of shares of common stock - basic

 

59,863,102

 

59,234,720

 

59,856,941

 

59,070,063

Weighted average number of shares of common stock - diluted

 

60,681,676

 

61,207,625

 

60,892,992

 

60,921,482

Securities outstanding that were included in the computation above, utilizing the treasury stock method are as follows:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Stock options, SARs, and RSUs to purchase common stock

818,574

1,972,905

1,036,051

1,851,419

Potential shares of common stock issuable that were excluded from the computation of diluted weighted-average shares outstanding excluded from the numerator, are as follows:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Stock options, SARs, and RSUs to purchase common stock

 

5,518,309

 

4,754,958

5,300,832

 

4,876,444

v3.23.3
Income Taxes
9 Months Ended
Sep. 30, 2023
Income Taxes  
Income Taxes

16. INCOME TAXES

A reconciliation between the statutory federal income tax rate and the Company’s effective income tax rate for the three and nine months ended September 30, 2023 and 2022 is as follows:

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

2023

    

2022

 

Federal income tax rate

21.0

%  

21.0

%

21.0

%  

21.0

%

Stock-based compensation

(17.0)

(0.9)

4.4

State taxes

4.0

(22.1)

4.7

 

(0.5)

Credits

0.2

(1.6)

(0.2)

Other

0.6

0.3

 

0.7

Valuation allowance

(985.7)

 

(144.9)

Total

25.8

%  

(1,003.8)

%

23.5

%  

(119.5)

%

v3.23.3
Related-party Transactions
9 Months Ended
Sep. 30, 2023
Related-party Transactions  
Related-party Transactions

17. RELATED-PARTY TRANSACTIONS

The Company was party to a management agreement for professional services provided by a related party, Paragon Biosciences, LLC (“Paragon”). The related party is an entity that shares common ownership with the Company. In addition, the Chairman of the Company’s board of directors was the President and owner of the entity. The Company terminated the management agreement upon the consummation of its IPO. The Company is also party to a right of use agreement with the related party whereby it has access to and the right to use certain office space leased by the related party in Chicago, IL. In addition, the Company had participated in certain transactions with separate related parties that also share common ownership with the Company, primarily related to combined employee health plans. The Company incurred $73 and $71 for the three months ended September 30, 2023 and 2022, and incurred $218 and $213 for the nine months ended September 30, 2023 and 2022, respectively, in expenses to this related party, which are included in general and administrative expense in the unaudited condensed consolidated statements of operations and comprehensive loss. As of September 30, 2023 and December 31, 2022, there were no amounts due to or due from related parties included in the unaudited condensed consolidated balance sheets.

v3.23.3
Subsequent Events
9 Months Ended
Sep. 30, 2023
Subsequent Events  
Subsequent Events

18. SUBSEQUENT EVENTS

On October 10, 2023, the Company completed a tender offer (the “Tender Offer”) to acquire all of the outstanding shares of common stock of Zynerba Pharmaceuticals, Inc. (“Zynerba Common Stock”), a clinical-stage pharmaceutical company focused on innovative pharmaceutically produced transdermal cannabidiol therapies for orphan neuropsychiatric disorders, including Fragile X syndrome.

Under the terms of the Tender Offer, the Company paid (i) $1.1059 per share of Zynerba Common Stock (the “Common Cash Amount”), plus (ii) one contingent value right (each, a “CVR”) per share of Zynerba Common Stock (the “Common CVR Amount”) for each holder of Zynerba Common Stock upon the closing of the Tender Offer, which represents the right to receive up to approximately $2.5444 per share of Zynerba Common Stock, subject to the achievement of certain clinical, regulatory and sales-based milestones. Both the Common Cash Amount and Common CVR Amount are to be paid in cash, subject to any applicable withholding of taxes and without interest. The aggregate consideration paid by the Company to acquire the Zynerba Common Stock upon completion of the Tender Offer was $60,000, exclusive of transaction related fees. The Company financed the acquisition with cash on hand.

On October 27, 2023, the Company’s Board of Directors approved a program providing for the repurchase of shares of common stock in an aggregate amount of up to $200,000, excluding commissions and transaction fees (the “October 2023 Repurchase Program”). The board simultaneously terminated the August 2023 Repurchase Program and any remaining amount authorized for the repurchase of shares. The October 2023 Repurchase Program may be suspended, terminated, or modified at any time for any reason.

v3.23.3
Summary of Significant Accounting Policies (Policies)
9 Months Ended
Sep. 30, 2023
Summary of Significant Accounting Policies  
Basis of Presentation

Basis of Presentation

The unaudited condensed consolidated financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”) and include all adjustments necessary for the fair presentation of the Company’s financial position for the periods presented. All intercompany accounts and transactions have been eliminated in consolidation. The unaudited condensed consolidated balance sheet as of September 30, 2023, the unaudited condensed consolidated statements of cash flows for the three and nine months ended September 30, 2023, and 2022, and the unaudited condensed consolidated statements of operations and comprehensive income and the unaudited condensed consolidated statements of shareholders’ equity for the three and nine months ended September 30, 2023 and 2022, are unaudited. The balance sheet as of December 31, 2022, was derived from audited financial statements as of and for the year ended December 31, 2022. The unaudited interim condensed consolidated financial statements have been prepared on the same basis as the audited annual financial statements as of and for the year ended December 31, 2022, and, in the opinion of management, reflect all adjustments, which include only normal recurring adjustments, necessary for the fair presentation of the Company’s financial position as of September 30, 2023, and the results of its operations and its cash flows for the three and nine months ended September 30, 2023 and 2022. The unaudited condensed consolidated results of operations are not necessarily indicative of the results that may occur for the full fiscal year. Certain information and disclosures normally included in the financial statements prepared in accordance with GAAP have been condensed or omitted under the SEC’s rules and regulations. These unaudited condensed consolidated financial statements should be read

in conjunction with the audited financial statements and accompanying notes thereto contained in the Company’s Annual Report on Form 10-K for the year ended December 31, 2022.

Use of Estimates

Use of Estimates

The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts and disclosures in the unaudited condensed consolidated financial statements, including the notes thereto, and elsewhere in this report. Actual results may differ significantly from estimates, which include rebates due pursuant to commercial and government contracts, accrued research and development expenses, stock-based compensation expense and income taxes.

Cash, Cash Equivalents and Restricted Cash

Cash, Cash Equivalents and Restricted Cash

Cash and cash equivalents and restricted cash consist of cash and, if applicable, highly liquid investments with an original maturity of three months or less when purchased, including investments in Money Market Funds and debt securities that approximate fair value. The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheet and the statements of cash flows.

    

As of

    

September 30, 

    

December 31, 

2023

2022

Cash and cash equivalents

$

324,603

$

243,784

Restricted cash

 

250

 

750

Total cash, cash equivalents, and restricted cash shown in the statements of cash flows

$

324,853

$

244,534

Restricted cash includes amounts required to be held as a security deposit in the form of letters of credit for the Company’s credit card program and the fleet program.

Investments

Investments

The Company’s investments consist of debt securities that are classified as available-for-sale. Short-term and long-term investments are carried at fair value and unrealized gains and losses are recorded as a component of accumulated comprehensive income in stockholders’ equity. The amortization of premiums and accretion of discounts adjust the carrying value of investments and are recorded in interest expense, net, on the unaudited condensed consolidated statements of operations and comprehensive income. Interest income and realized gains and losses, if any, are also recorded in interest expense, net, on the unaudited condensed consolidated statement of operations and comprehensive income. Realized gains and losses that result from the sale of investments are determined on a specific identification basis.

At each reporting period, the Company reviews any unrealized losses position to determine if the decline in the fair value of the underlying investments is a result of credit losses or other factors. If the assessment indicates that a credit loss exists, any impairment is recognized as an allowance for credit losses in our consolidated statement of operations.

Interest income generated from our investments and cash equivalents, which is included in interest expense, net, was $3,384 and $8,537 for the three and nine months ended September 30, 2023, respectively, compared to $828 and $1,145 for the three and nine months ended September 30, 2022, respectively.

Concentrations of Risk

Concentrations of Risk

Substantially all of the Company’s cash and money market funds are held in four financial institutions. Due to their size, the Company believes these financial institutions represent minimal credit risk. Deposits may

exceed the amount of insurance provided on such deposits by the Federal Deposit Insurance Corporation for U.S. institutions. The Company has not experienced any losses on its deposits of cash and cash equivalents. The Company believes that it is not exposed to significant credit risk due to the financial position of the depository institutions in which those deposits are held.

The Company is subject to credit risk from its trade receivables related to its product sales. The Company extends credit to specialty pharmaceutical distribution companies within the United States. Customer creditworthiness is monitored, and collateral is not required. Historically, the Company has not experienced credit losses on its accounts receivable. The Company monitors its exposure within accounts receivable and would record a reserve against uncollectible accounts receivable if necessary. As of September 30, 2023, three customers accounted for 100% of gross accounts receivable; Caremark LLC (“CVS Caremark”), which accounted for 37% of gross accounts receivable; Accredo Health Group, Inc. (“Accredo”), which accounted for 37% of gross accounts receivable; and PANTHERx Specialty Pharmacy LLC (“Pantherx”), which accounted for 26% of gross accounts receivable. As of December 31, 2022, three customers accounted for 100% of gross accounts receivable; CVS Caremark, which accounted for 41% of gross accounts receivable, Accredo, which accounted for 35% of gross accounts receivable; and Pantherx, which accounted for 24% of gross accounts receivable.

For the nine months ended September 30, 2023, three customers accounted for 100% of gross product revenues; CVS Caremark accounted for 37% of gross product revenues; Accredo accounted for 32% of gross product revenues; and Pantherx accounted for 31% of gross product revenues. For the nine months ended September 30, 2022, three customers accounted for 100% of gross product revenues; CVS Caremark accounted for 40% of gross product revenues; Pantherx accounted for 30% of gross product revenues; and Accredo accounted for 30% of gross product revenues.

The Company depends on a single source supplier for each of its product and active pharmaceutical ingredient.

Share Repurchases

Share Repurchases

The Company accounts for share repurchases as constructive retirements, whereby it reduces common stock and additional paid-in capital by the amount of the original issuance, with any excess purchase price recorded as a reduction to retained earnings. Under this method, issued and outstanding shares of common stock are reduced by the amount of shares of common stock repurchased, and no treasury stock is recognized on the condensed consolidated financial statements.

Recently Issued Accounting Pronouncements

Recently Issued Accounting Pronouncements

The Company did not adopt any new accounting pronouncements that had a material effect on its condensed consolidated financial statements during the three and nine months ended September 30, 2023.

v3.23.3
Summary of Significant Accounting Policies (Tables)
9 Months Ended
Sep. 30, 2023
Summary of Significant Accounting Policies  
Schedule of reconciliation of cash, cash equivalents, and restricted cash The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheet and the statements of cash flows.

    

As of

    

September 30, 

    

December 31, 

2023

2022

Cash and cash equivalents

$

324,603

$

243,784

Restricted cash

 

250

 

750

Total cash, cash equivalents, and restricted cash shown in the statements of cash flows

$

324,853

$

244,534

v3.23.3
Investments (Tables)
9 Months Ended
Sep. 30, 2023
Investments  
Schedule of carrying value and amortized cost of available-for-sale debt securities

The carrying value and amortized cost of the Company’s available-for-sale debt securities, summarized by type of security, consisted of the following:

September 30, 2023

Amortized

Unrealized

Unrealized

Fair

Cost

Gains

Losses

Value

Short-term:

Commercial paper

$

27,717

1

(13)

$

27,705

Corporate debt securities

16,456

3

(7)

16,452

U.S. government securities

1,915

(1)

1,914

Total short-term investments

$

46,088

4

(21)

$

46,071

Long-term:

Commercial paper

$

1,623

(2)

$

1,621

Corporate debt securities

39,497

14

(155)

39,356

U.S. government securities

27,079

(356)

26,723

Total long-term investments

$

68,199

14

(513)

$

67,700

December 31, 2022

Amortized

Unrealized

Unrealized

Fair

Cost

Gains

Losses

Value

Short-term:

Commercial paper

$

26,553

15

(34)

$

26,534

Corporate debt securities

49,213

9

(73)

49,149

U.S. government securities

3,658

(10)

3,648

Total short-term investments

$

79,424

24

(117)

$

79,331

Long-term:

Commercial paper

$

853

1

$

854

Corporate debt securities

21,516

11

(68)

21,459

U.S. government securities

257

(2)

255

Total long-term investments

$

22,626

12

(70)

$

22,568

v3.23.3
Fair Value Measurements (Tables)
9 Months Ended
Sep. 30, 2023
Fair Value Measurements  
Schedule of assets measured at fair value

The Company’s assets measured at fair value consisted of the following:

September 30, 2023

December 31, 2022

Total

Level 1

Level 2

Total

Level 1

Level 2

Assets

Cash equivalents

$

198,135

198,135

$

184,977

184,977

Commercial paper

29,326

29,326

27,388

27,388

Corporate debt securities

55,808

55,808

70,608

70,608

U.S. government securities

28,637

28,637

3,903

3,903

Total

$

311,906

198,135

113,771

$

286,876

184,977

101,899

v3.23.3
Inventory (Tables)
9 Months Ended
Sep. 30, 2023
Inventory  
Schedule of inventory net

Inventory, net consisted of the following:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Raw materials

$

932

$

838

Work in process

 

1,833

 

1,513

Finished goods

 

2,611

 

2,565

Inventory, gross

 

5,376

 

4,916

Reserve for excess inventory

 

(289)

 

(619)

Total inventory, net

$

5,087

$

4,297

v3.23.3
Intangible Assets (Tables)
9 Months Ended
Sep. 30, 2023
Intangible Assets  
Schedule of expected future annual amortization expense for unamortized intangible assets

The Company expects the future annual amortization expense for the unamortized intangible assets to be as follows:

Years ending December 31, 

    

2023 (Excluding the nine months ended September 30, 2023)

$

5,961

2024

 

23,845

2025

 

23,845

2026

 

23,845

2027

 

23,845

Thereafter

41,728

Total

$

143,069

Schedule of gross carrying amount and net book value of intangible assets

The gross carrying amount and net book value of the intangible asset is as follows:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Gross Carrying Amount

$

215,000

$

215,000

Accumulated Amortization

 

(71,931)

 

(54,047)

Net Book Value

$

143,069

$

160,953

v3.23.3
Accrued Expenses (Tables)
9 Months Ended
Sep. 30, 2023
Accrued Expenses  
Schedule of accrued expenses

Accrued expenses consist of the following:

    

As of

    

September 30, 

    

December 31, 

2023

2022

Royalties due to Bioprojet

$

29,665

$

25,367

Rebates and other sales deductions

 

31,853

 

27,860

Interest

3,140

3,286

Selling and marketing

 

2,253

 

1,135

Research and development

 

2,190

 

358

Professional fees, consulting, and other services

 

1,841

 

1,163

Other expenses

 

1,819

 

773

$

72,761

$

59,942

v3.23.3
Debt (Tables)
9 Months Ended
Sep. 30, 2023
Debt  
Schedule of long-term debt, net

Long-term debt, net consists of the following:

    

September 30, 

    

December 31, 

2023

2022

Liability component - principal

$

200,000

$

197,500

Unamortized debt discount associated with debt financing costs

 

(2,869)

 

(5,853)

Liability component - net carrying value

197,131

191,647

Less current portion

(15,000)

(2,000)

Long-term debt, net

$

182,131

$

189,647

Schedule of future minimum payments relating to long term debt

Future minimum payments relating to long-term debt, net as of September 30, 2023, for the periods indicated below consists of the following:

Years ending December 31, 

2023 (Excluding the nine months ended September 30, 2023)

$

3,750

2024

 

15,000

2025

 

16,250

2026

 

20,000

2027

 

20,000

Thereafter

125,000

Total

$

200,000

Schedule of interest expense related to long term debt

Interest expense related to the Company’s long-term debt, net, is included in interest expense, net in the unaudited condensed consolidated statements of operations and comprehensive income and consists of the following:

Three Months Ended

Nine Months Ended

September 30, 

September 30, 

2023

    

2022

2023

    

2022

Interest on principal balance

$

4,791

$

4,513

$

15,900

$

12,110

Amortization of deferred financing costs

 

2,221

 

418

 

3,061

 

1,241

Total term loan interest expense

$

7,012

$

4,931

$

18,961

$

13,351

v3.23.3
Leases (Tables)
9 Months Ended
Sep. 30, 2023
Leases  
Schedule of supplemental balance sheet and cash flow information related to operating leases

Supplemental balance sheet information related to operating leases was as follows:

Leases

Classification

September 30, 2023

  

December 31, 2022

Assets

Operating lease right-of-use assets

Other noncurrent assets

$

2,456

$

2,312

Liabilities

Operating lease liability, current portion

Other current liabilities

$

1,683

$

1,614

Operating lease liability, long-term

Other long-term liabilities

901

975

Total operating lease liabilities

$

2,584

$

2,589

Supplemental cash flow information related to operating leases was as follows:

September 30, 2023

September 30, 2022

Operating cash flows from operating leases

$

1,448

$

1,297

Right of use assets obtained in exchange for operating lease obligations

$

1,592

$

485

Schedule of future payments under noncancelable operating leases

Future payments under noncancelable operating leases with initial terms of one year or more as of September 30, 2023 consisted of the following:

Years ending December 31, 

    

2023 (Excluding the nine months ended September 30, 2023)

$

558

2024

 

1,407

2025

 

532

2026

 

252

2027

 

Thereafter

 

Total lease payments

2,749

Less: imputed interest

(165)

Total lease liabilities

$

2,584

v3.23.3
Stock Incentive Plan and Stock-based Compensation (Tables)
9 Months Ended
Sep. 30, 2023
Stock Incentive Plan and Stock-based Compensation  
Summary of changes in stock options granted

The following table summarizes stock option activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Exercise

Contractual

    

Awards

    

Price

    

Term

Awards outstanding—December 31, 2022

 

6,460,947

$

30.90

 

7.86

Awards issued

 

376,422

$

36.71

 

  

Awards exercised

 

(367,376)

$

12.02

 

  

Awards forfeited

 

(206,318)

$

24.84

 

  

Awards outstanding—September 30, 2023

 

6,263,675

$

32.55

 

7.39

Summary of changes in SARs granted

The following table summarizes SARs activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Exercise

Contractual

    

Awards

    

Price

    

Term

Awards outstanding—December 31, 2022

 

43,208

$

9.38

 

6.32

Awards issued

 

$

 

  

Awards exercised

 

$

 

  

Awards forfeited

 

$

 

  

Awards outstanding—September 30, 2023

 

43,208

$

9.38

 

5.58

Summary of changes in RSUs granted

The following table summarizes RSU activity for the nine months ended September 30, 2023:

    

    

    

Weighted-

Weighted-

Average

Average

Remaining

Number of

Grant Date

Contractual

    

Awards

    

Fair Value

    

Term

Awards outstanding—December 31, 2022

 

60,000

$

29.03

 

8.24

Awards issued

 

$

 

  

Awards vested

 

(30,000)

$

29.03

 

  

Awards forfeited

 

$

 

  

Awards outstanding—September 30, 2023

 

30,000

$

29.03

 

7.49

Summary of assumptions used to value awards

The assumptions used to value the awards are summarized in the following table.

As of

    

September 30, 

    

December 31, 

    

2023

    

2022

Dividend yield

 

0.00

%  

0.00

%

Expected volatility

 

76.32 - 80.21

%  

72.57 - 77.08

%

Risk-free interest rate

 

3.42 - 4.61

%  

1.99 - 4.05

%

Lack of marketability discount

 

0.00

%  

0.00

%

Expected term (years)

 

2.4 - 6.3

 

3.1 - 6.3

Summary of stock-based compensation expense

Stock-based compensation expense, net for the three and nine months ended September 30, 2023 and 2022, was recorded in the unaudited condensed consolidated statements of operations and comprehensive income in the following line items:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

    

2023

    

2022

    

2023

    

2022

Research and development expense

$

1,030

$

522

$

2,962

$

1,866

Sales and marketing expense

 

1,218

 

1,096

 

3,437

 

2,956

General and administrative expense

 

5,709

 

5,349

 

15,912

 

14,412

$

7,957

$

6,967

$

22,311

$

19,234

v3.23.3
Earnings per Share (Tables)
9 Months Ended
Sep. 30, 2023
Earnings per Share  
Summary of computation of basic and diluted net income (loss) per share

The following table sets forth the computation of basic and diluted net income per share:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Numerator

 

  

 

  

  

 

  

Net income

$

38,461

$

87,943

$

102,246

$

132,959

Denominator

 

  

 

  

 

  

 

  

Net income per share of common stock - basic

$

0.64

$

1.48

$

1.71

$

2.25

Net income per share of common stock- diluted

$

0.63

$

1.44

$

1.68

$

2.18

Weighted average number of shares of common stock - basic

 

59,863,102

 

59,234,720

 

59,856,941

 

59,070,063

Weighted average number of shares of common stock - diluted

 

60,681,676

 

61,207,625

 

60,892,992

 

60,921,482

Summary of antidilutive securities excluded from computation of earnings per share

Securities outstanding that were included in the computation above, utilizing the treasury stock method are as follows:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Stock options, SARs, and RSUs to purchase common stock

818,574

1,972,905

1,036,051

1,851,419

Potential shares of common stock issuable that were excluded from the computation of diluted weighted-average shares outstanding excluded from the numerator, are as follows:

    

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

    

2023

    

2022

Stock options, SARs, and RSUs to purchase common stock

 

5,518,309

 

4,754,958

5,300,832

 

4,876,444

v3.23.3
Income Taxes (Tables)
9 Months Ended
Sep. 30, 2023
Income Taxes  
Schedule of reconciliation between statutory federal income tax rate and the Company's effective income tax rate

Three Months Ended September 30, 

Nine Months Ended September 30, 

2023

    

2022

2023

    

2022

 

Federal income tax rate

21.0

%  

21.0

%

21.0

%  

21.0

%

Stock-based compensation

(17.0)

(0.9)

4.4

State taxes

4.0

(22.1)

4.7

 

(0.5)

Credits

0.2

(1.6)

(0.2)

Other

0.6

0.3

 

0.7

Valuation allowance

(985.7)

 

(144.9)

Total

25.8

%  

(1,003.8)

%

23.5

%  

(119.5)

%

v3.23.3
Liquidity and Capital Resources (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Liquidity And Capital Resources    
Accumulated deficit $ 169,884 $ 272,130
Cash, cash equivalents and investments $ 438,374  
v3.23.3
Summary of Significant Accounting Policies - Schedule of Reconciliation of Cash, Cash Equivalents, and Restricted Cash (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Sep. 30, 2022
Dec. 31, 2021
Summary of Significant Accounting Policies        
Cash and cash equivalents $ 324,603 $ 243,784    
Restricted cash 250 750    
Total cash, cash equivalents, and restricted cash shown in the statements of cash flows $ 324,853 $ 244,534 $ 262,093 $ 235,059
v3.23.3
Summary of Significant Accounting Policies - Additional Information (Details)
$ in Thousands
3 Months Ended 9 Months Ended 12 Months Ended
Sep. 30, 2023
USD ($)
Sep. 30, 2022
USD ($)
Sep. 30, 2023
USD ($)
customer
Institution
Sep. 30, 2022
USD ($)
customer
Dec. 31, 2022
customer
Summary Of Significant Accounting Policies [Line Items]          
Number Of financial institutions | Institution     4    
Investment income, interest | $ $ 3,384 $ 828 $ 8,537 $ 1,145  
Three Customers | Accounts Receivable | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Number of customers     3   3
Concentration risk percentage     100.00%   100.00%
Three Customers | Product Revenues | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Number of customers     3 3  
Concentration risk percentage     100.00% 100.00%  
Caremark LLC | Accounts Receivable | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Concentration risk percentage     37.00%   41.00%
Caremark LLC | Product Revenues | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Concentration risk percentage     37.00% 40.00%  
Accredo Health Group, Inc | Accounts Receivable | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Concentration risk percentage     37.00%   35.00%
Accredo Health Group, Inc | Product Revenues | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Concentration risk percentage     32.00% 30.00%  
PANTHERx Specialty Pharmacy LLC | Accounts Receivable | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Concentration risk percentage     26.00%   24.00%
PANTHERx Specialty Pharmacy LLC | Product Revenues | Customer Concentration Risk          
Summary Of Significant Accounting Policies [Line Items]          
Concentration risk percentage     31.00% 30.00%  
v3.23.3
Investments - Carrying Value and Amortized Cost of Available-For-Sale Debt Securities (Details) - USD ($)
$ in Thousands
9 Months Ended
Sep. 30, 2023
Dec. 31, 2022
Minimum    
Investment securities    
Non current investment maturity term 1 year  
Maximum    
Investment securities    
Non current investment maturity term 2 years  
Short-term    
Investment securities    
Amortized Cost $ 46,088 $ 79,424
Unrealized Gains 4 24
Unrealized Losses (21) (117)
Fair Value 46,071 79,331
Short-term commercial paper    
Investment securities    
Amortized Cost 27,717 26,553
Unrealized Gains 1 15
Unrealized Losses (13) (34)
Fair Value 27,705 26,534
Short-term corporate debt securities    
Investment securities    
Amortized Cost 16,456 49,213
Unrealized Gains 3 9
Unrealized Losses (7) (73)
Fair Value 16,452 49,149
Short-term U.S. government securities    
Investment securities    
Amortized Cost 1,915 3,658
Unrealized Losses (1) (10)
Fair Value 1,914 3,648
Long-term    
Investment securities    
Amortized Cost 68,199 22,626
Unrealized Gains 14 12
Unrealized Losses (513) (70)
Fair Value 67,700 22,568
Long-term commercial paper    
Investment securities    
Amortized Cost 1,623 853
Unrealized Gains   1
Unrealized Losses (2)  
Fair Value 1,621 854
Long-term corporate debt securities    
Investment securities    
Amortized Cost 39,497 21,516
Unrealized Gains 14 11
Unrealized Losses (155) (68)
Fair Value 39,356 21,459
Long-term U.S. government securities    
Investment securities    
Amortized Cost 27,079 257
Unrealized Losses (356) (2)
Fair Value $ 26,723 $ 255
v3.23.3
Fair Value Measurements - Assets Measured at Fair Value (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Assets    
Assets $ 311,906 $ 286,876
Cash equivalents    
Assets    
Assets 198,135 184,977
Commercial paper    
Assets    
Assets 29,326 27,388
Corporate debt securities    
Assets    
Assets 55,808 70,608
U.S. government securities    
Assets    
Assets 28,637 3,903
Level 1    
Assets    
Assets 198,135 184,977
Level 1 | Cash equivalents    
Assets    
Assets 198,135 184,977
Level 2    
Assets    
Assets 113,771 101,899
Level 2 | Commercial paper    
Assets    
Assets 29,326 27,388
Level 2 | Corporate debt securities    
Assets    
Assets 55,808 70,608
Level 2 | U.S. government securities    
Assets    
Assets $ 28,637 $ 3,903
v3.23.3
Inventory (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Inventory    
Raw materials $ 932 $ 838
Work in process 1,833 1,513
Finished goods 2,611 2,565
Inventory, gross 5,376 4,916
Reserve for excess inventory (289) (619)
Total inventory, net $ 5,087 $ 4,297
v3.23.3
Intangible Assets - Additional Information (Details) - USD ($)
$ in Thousands
1 Months Ended 3 Months Ended 9 Months Ended
Mar. 31, 2022
Feb. 28, 2022
Jan. 31, 2021
Aug. 31, 2019
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Intangible Assets                
Amortization expense         $ 5,962 $ 5,961 $ 17,884 $ 17,005
Net product revenues         $ 160,268 $ 117,206 $ 413,610 $ 309,547
WAKIX                
Intangible Assets                
Final payment paid $ 40,000              
Useful life of intangible asset         7 years 7 months 6 days   7 years 7 months 6 days  
Remaining useful life         6 years   6 years  
WAKIX | United States                
Intangible Assets                
Net product revenues   $ 500,000            
WAKIX | Daytime Sleepiness                
Intangible Assets                
License agreement milestone payments paid       $ 75,000        
Useful life of intangible asset         10 years   10 years  
Remaining useful life         6 years   6 years  
NDA for WAKIX. | Cataplexy                
Intangible Assets                
License agreement milestone payments paid     $ 100,000          
Useful life of intangible asset         9 years   9 years  
Remaining useful life         6 years   6 years  
v3.23.3
Intangible Assets - Schedule of Expected Future Annual Amortization Expense for Unamortized Intangible Assets (Details)
$ in Thousands
Sep. 30, 2023
USD ($)
Future annual amortization expense  
2023 (Excluding the nine months ended September 30, 2023) $ 5,961
2024 23,845
2025 23,845
2026 23,845
2027 23,845
Thereafter 41,728
Total $ 143,069
v3.23.3
Intangible Assets - Schedule of Gross Carrying Amount and Net Book Value of Intangible Assets (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Intangible Assets    
Gross Carrying Amount $ 215,000 $ 215,000
Accumulated Amortization (71,931) (54,047)
Net Book Value $ 143,069 $ 160,953
v3.23.3
License Agreements and Asset Purchase Agreements (Details) - USD ($)
$ in Thousands
1 Months Ended 3 Months Ended 9 Months Ended
Mar. 31, 2023
Jul. 31, 2022
Aug. 31, 2021
Jan. 31, 2021
Oct. 31, 2020
Nov. 30, 2019
Aug. 31, 2019
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Dec. 31, 2022
Feb. 28, 2019
License Agreements and Asset Purchase Agreements                          
Cost of product sold               $ 32,296 $ 22,959 $ 78,084 $ 56,596    
Accrued Sales Based Trademark and Royalties               29,665   29,665   $ 25,367  
All Countries Excluding Greater China | HBS-102 | Asset Purchase Agreement with ConSynance Therapeutics                          
License Agreements and Asset Purchase Agreements                          
Consideration transferred     $ 3,500                    
Payment for intellectual property upon preclinical milestones     1,000                    
Payment for intellectual property upon developmental milestones     19,000                    
Payment for intellectual property upon regulatory milestones     44,000                    
Payment for intellectual property upon sales milestones     $ 110,000                    
All Countries Excluding Greater China | HBS-102 | Asset Purchase Agreement with ConSynance Therapeutics | Research and Development Expense                          
License Agreements and Asset Purchase Agreements                          
Payment related to achievement of preclinical milestone. $ 750,000                        
Bioprojet                          
License Agreements and Asset Purchase Agreements                          
Licensing agreement milestone fees             $ 2,000            
License agreement milestone payments paid           $ 75,000 2,000            
License agreement, additional milestone payment due             102,000            
Accrued Sales Based Trademark and Royalties               29,665   29,665   $ 25,367  
Bioprojet | Upon Acceptance by FDA of Pitolisant's                          
License Agreements and Asset Purchase Agreements                          
License agreement, milestone payment due                         $ 50,000
License agreement, upfront non-refundable licensing fees paid   $ 30,000                      
License agreement, maximum additional milestone payment due   $ 155,000                      
Bioprojet | Upon FDA Approval of WAKIX                          
License Agreements and Asset Purchase Agreements                          
License agreement, milestone payment due             77,000            
Licensing agreement milestone fees             $ 2,000            
License agreement milestone payments paid       $ 100,000 $ 2,000                
Bioprojet | Sales-based, trademark and tiered royalties                          
License Agreements and Asset Purchase Agreements                          
Cost of product sold               $ 29,665 $ 20,944 71,267 $ 51,741    
Bioprojet | United States                          
License Agreements and Asset Purchase Agreements                          
Amount of Aggregate Net Sales Attaining                   500,000      
Bioprojet | Attaining $500,000 Aggregate Net Sales | United States | Upon FDA Approval of WAKIX                          
License Agreements and Asset Purchase Agreements                          
Final payment paid                   $ 40,000      
v3.23.3
Accrued Expenses (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Accrued Expenses    
Royalties due to Bioprojet $ 29,665 $ 25,367
Rebates and other sales deductions 31,853 27,860
Interest 3,140 3,286
Selling and marketing 2,253 1,135
Research and development 2,190 358
Professional fees, consulting, and other services 1,841 1,163
Other expenses 1,819 773
Accrued expenses $ 72,761 $ 59,942
v3.23.3
Debt - Additional Information (Details) - USD ($)
$ in Thousands
1 Months Ended 3 Months Ended 9 Months Ended
Jul. 26, 2023
Aug. 10, 2022
Aug. 31, 2021
Sep. 30, 2023
Sep. 30, 2023
Sep. 21, 2023
DEBT            
Debt issuance costs paid         $ 2,997  
Loss on debt extinguishment       $ 9,766 9,766  
Blackstone Alternative Credit Advisors ("Blackstone")            
DEBT            
Extinguishment of loan, amount         207,308  
Loss on debt extinguishment         9,766  
Unamortized debt issuance costs       1,972 1,972  
Term Loans            
DEBT            
Debt issuance costs       2,997 2,997  
Net cash received         197,003  
Fair value of loan       $ 199,820 199,820  
Term Loans | Repayment Of Debt Commencing On December 31 2023            
DEBT            
Periodic payment principal         3,750  
Term Loans | Repayment Of Debt Beginning On December 31 2025            
DEBT            
Periodic payment principal         5,000  
Term Loans | Repayment of Debt Due on Maturity Date of July 26, 2028            
DEBT            
Periodic payment principal         $ 115,000  
Term Loans | Base rate | Minimum            
DEBT            
Basis spread on variable rate         2.50%  
Term Loans | Base rate | Maximum            
DEBT            
Basis spread on variable rate         3.00%  
Term Loans | SOFR            
DEBT            
Credit spread adjustment rate         0.10%  
Term Loans | SOFR | Minimum            
DEBT            
Basis spread on variable rate         3.50%  
Term Loans | SOFR | Maximum            
DEBT            
Basis spread on variable rate         4.00%  
TLA Term Loan            
DEBT            
Term of loan 5 years          
Aggregate principal amount $ 185,000          
Incremental Term Loan            
DEBT            
Aggregate principal amount           $ 15,000
Senior Secured Term Loan | Blackstone Alternative Credit Advisors ("Blackstone")            
DEBT            
Aggregate principal amount     $ 200,000      
Debt issuance costs     8,151      
Net cash received     191,849      
Senior Secured Delayed Draw Term Loan | Blackstone Alternative Credit Advisors ("Blackstone")            
DEBT            
Aggregate principal amount     100,000      
Percentage of ticking fee   1.00%        
Debt issuance costs paid     $ 1,000      
v3.23.3
Debt - Balances of Long-term Debt, Net (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Debt    
Liability component - principal $ 200,000 $ 197,500
Unamortized debt discount associated with debt financing costs (2,869) (5,853)
Liability component - net carrying value 197,131 191,647
Less current portion (15,000) (2,000)
Long-term debt, net $ 182,131 $ 189,647
v3.23.3
Debt - Future Minimum Payments (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Future minimum payments    
2023 (Excluding the nine months ended September 30, 2023) $ 3,750  
2024 15,000  
2025 16,250  
2026 20,000  
2027 20,000  
Thereafter 125,000  
Total $ 200,000 $ 197,500
v3.23.3
Debt - Interest Expense (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Debt        
Interest on principal balance $ 4,791 $ 4,513 $ 15,900 $ 12,110
Amortization of deferred financing costs 2,221 418 3,061 1,241
Total term loan interest expense $ 7,012 $ 4,931 $ 18,961 $ 13,351
v3.23.3
Leases (Details)
ft² in Thousands, $ in Thousands
1 Months Ended 3 Months Ended 9 Months Ended
Jun. 30, 2018
ft²
Sep. 30, 2023
USD ($)
Sep. 30, 2022
USD ($)
Sep. 30, 2023
USD ($)
Sep. 30, 2022
USD ($)
LEASES          
Operating lease square feet of office space 15        
Additional office space leased one 13        
Additional office space leased two 7        
Lessee, Operating Lease, Existence of Option to Extend [true false]       true  
Lessee, Operating Lease, Existence of Option to Terminate [true false]       true  
Cost operating lease | $   $ 473 $ 378 $ 1,295 $ 1,155
Weighted average remaining lease term   1 year 9 months 18 days   1 year 9 months 18 days  
Weighted-average discount rate for operating leases   6.00%   6.00%  
Minimum          
LEASES          
Lease terms   1 year   1 year  
Maximum          
LEASES          
Lease terms   3 years   3 years  
v3.23.3
Leases - Supplemental Balance Sheet Information (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Assets    
Operating lease right-of-use assets $ 2,456 $ 2,312
Operating Lease, Right-of-Use Asset, Statement of Financial Position [Extensible Enumeration] Other Assets Noncurrent Other Assets Noncurrent
Liabilities    
Operating lease liability, current portion $ 1,683 $ 1,614
Operating Lease, Liability, Current, Statement of Financial Position [Extensible Enumeration] Other Liabilities Current Other Liabilities Current
Operating lease liability, long-term $ 901 $ 975
Operating Lease, Liability, Noncurrent, Statement of Financial Position [Extensible Enumeration] Other Liabilities Noncurrent Other Liabilities Noncurrent
Total operating lease liabilities $ 2,584 $ 2,589
v3.23.3
Leases - Supplemental Cash Flow Information (Details) - USD ($)
$ in Thousands
9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Leases    
Operating cash flows from operating leases $ 1,448 $ 1,297
Right of use assets obtained in exchange for operating lease obligations $ 1,592 $ 485
v3.23.3
Leases - Future Payments (Details) - USD ($)
$ in Thousands
Sep. 30, 2023
Dec. 31, 2022
Years ending December 31,    
2023 (Excluding the nine months ended September 30, 2023) $ 558  
2024 1,407  
2025 532  
2026 252  
Total lease payments 2,749  
Less: imputed interest (165)  
Total operating lease liabilities $ 2,584 $ 2,589
v3.23.3
Stockholders' Equity (Details)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
USD ($)
Vote
shares
Sep. 30, 2023
USD ($)
Vote
shares
Aug. 01, 2023
USD ($)
Equity, Class of Treasury Stock [Line Items]      
Number of votes for each common stock | Vote 1 1  
August 2023 Repurchase Program      
Equity, Class of Treasury Stock [Line Items]      
Repurchase of shares of common stock approved     $ 125,000
Repurchase and cancellation of common shares, Shares | shares 1,439,792 1,439,792  
Aggregate cost of common stock repurchased and cancelled, exclusive of commissions and transaction fees $ 50,000 $ 50,000  
Remaining authorized repurchase amount $ 75,000 $ 75,000  
v3.23.3
Stock Incentive Plan and Stock-based Compensation - Additional Information (Details) - USD ($)
$ / shares in Units, $ in Thousands
3 Months Ended 9 Months Ended 12 Months Ended
Apr. 30, 2021
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Dec. 31, 2022
Stock Incentive Plan and Stock-based Compensation            
Unrecognized stock-based compensation expense   $ 67,842   $ 67,842    
Weighted average period       2 years 4 months 24 days    
Shares issued under the ESPP   0 0 14,043 14,889  
2020 Plan            
Stock Incentive Plan and Stock-based Compensation            
Stock options contractual term       10 years    
Percentage of increment of common stock outstanding       4.00%    
Total number of shares available for issuance   6,755,091   6,755,091    
2017 and 2020 Plans | Restricted Stock Units            
Stock Incentive Plan and Stock-based Compensation            
Weighted average per share fair value of awards issued (in USD per share)       $ 20.13   $ 18.88
2017 and 2020 Plans | Common Stock            
Stock Incentive Plan and Stock-based Compensation            
Stock vested       3,141,836   1,818,045
Employee Stock Purchase Plan            
Stock Incentive Plan and Stock-based Compensation            
Percentage of increment of common stock outstanding 1.00%          
ESPP permits eligible employees to purchase shares of common stock at discount 15.00%          
Total number of shares available for issuance 629,805          
Amount of discount on ESSP   $ 100 $ 86 $ 308 $ 271  
v3.23.3
Stock Incentive Plan and Stock-based Compensation - Summary of Changes in Stock Options Granted (Details) - $ / shares
9 Months Ended 12 Months Ended
Sep. 30, 2023
Dec. 31, 2022
Stock Incentive Plan and Stock-based Compensation    
Number of Awards, Awards outstanding, Beginning balance 6,460,947  
Number of Awards, Awards issued 376,422  
Number of Awards, Awards exercised (367,376)  
Number of Awards, Awards forfeited (206,318)  
Number of Awards, Awards outstanding, Ending balance 6,263,675 6,460,947
Weighted-Average Exercise Price, Awards outstanding, Beginning balance $ 30.90  
Weighted-Average Exercise Price, Awards issued 36.71  
Weighted-Average Exercise Price, Awards exercised 12.02  
Weighted-Average Exercise Price, Awards forfeited 24.84  
Weighted-Average Exercise Price, Awards outstanding, Ending balance $ 32.55 $ 30.90
Weighted-Average Remaining Contractual Term 7 years 4 months 20 days 7 years 10 months 9 days
v3.23.3
Stock Incentive Plan and Stock-based Compensation - Summary of Changes in SARs Granted (Details) - Stock Appreciation Rights (SARs) [Member] - $ / shares
9 Months Ended 12 Months Ended
Sep. 30, 2023
Dec. 31, 2022
Share Based Compensation Arrangement By Share Based Payment Award [Line Items]    
Number of Awards, Awards outstanding, Beginning balance 43,208  
Number of Awards, Awards outstanding, Ending balance 43,208 43,208
Weighted-Average Exercise Price, Awards outstanding, Beginning balance $ 9.38  
Weighted-Average Exercise Price, Awards outstanding, Ending balance $ 9.38 $ 9.38
Weighted-Average Remaining Contractual Term 5 years 6 months 29 days 6 years 3 months 25 days
v3.23.3
Stock Incentive Plan and Stock-based Compensation - Summary of Changes in RSUs Granted (Details) - Restricted Stock Units - $ / shares
9 Months Ended 12 Months Ended
Sep. 30, 2023
Dec. 31, 2022
Share Based Compensation Arrangement By Share Based Payment Award [Line Items]    
Number of Awards, Awards outstanding, Beginning balance 60,000  
Number of Awards, Awards vested (30,000)  
Number of Awards, Awards outstanding, Ending balance 30,000 60,000
Weighted-Average Exercise Price, Awards outstanding, Beginning balance $ 29.03  
Weighted-Average Exercise Price, Awards vested 29.03  
Weighted-Average Exercise Price, Awards outstanding, Ending balance $ 29.03 $ 29.03
Weighted-Average Remaining Contractual Term 7 years 5 months 26 days 8 years 2 months 26 days
v3.23.3
Stock Incentive Plan and Stock-based Compensation - Summary of Assumptions Used to Value Awards (Details)
9 Months Ended 12 Months Ended
Sep. 30, 2023
Dec. 31, 2022
Share Based Compensation Arrangement By Share Based Payment Award [Line Items]    
Dividend yield 0.00% 0.00%
Expected volatility, minimum 76.32% 72.57%
Expected volatility, maximum 80.21% 77.08%
Risk-free interest rate, minimum 3.42% 1.99%
Risk-free interest rate, maximum 4.61% 4.05%
Lack of marketability discount 0.00% 0.00%
Minimum    
Share Based Compensation Arrangement By Share Based Payment Award [Line Items]    
Expected term (years) 2 years 4 months 24 days 3 years 1 month 6 days
Maximum    
Share Based Compensation Arrangement By Share Based Payment Award [Line Items]    
Expected term (years) 6 years 3 months 18 days 6 years 3 months 18 days
v3.23.3
Stock Incentive Plan and Stock-based Compensation - Summary of Stock-based Compensation Expense (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Employee Service Share Based Compensation Allocation Of Recognized Period Costs [Line Items]        
Stock-based compensation expense $ 7,957 $ 6,967 $ 22,311 $ 19,234
Research and Development Expense        
Employee Service Share Based Compensation Allocation Of Recognized Period Costs [Line Items]        
Stock-based compensation expense 1,030 522 2,962 1,866
Sales and Marketing Expense        
Employee Service Share Based Compensation Allocation Of Recognized Period Costs [Line Items]        
Stock-based compensation expense 1,218 1,096 3,437 2,956
General and Administrative Expense        
Employee Service Share Based Compensation Allocation Of Recognized Period Costs [Line Items]        
Stock-based compensation expense $ 5,709 $ 5,349 $ 15,912 $ 14,412
v3.23.3
Earnings per Share - Summary of Computation of Basic and Diluted Net Income (Loss) per Share (Details) - USD ($)
$ / shares in Units, $ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Numerator        
Net Income (Loss) $ 38,461 $ 87,943 $ 102,246 $ 132,959
Denominator        
Net income per share of common stock - basic $ 0.64 $ 1.48 $ 1.71 $ 2.25
Net income per share of common stock - diluted $ 0.63 $ 1.44 $ 1.68 $ 2.18
Weighted average number of shares of common stock - basic 59,863,102 59,234,720 59,856,941 59,070,063
Weighted average number of shares of common stock - diluted 60,681,676 61,207,625 60,892,992 60,921,482
v3.23.3
Earnings per Share - Summary of Securities Outstanding Included in Computation above, Utilizing Treasury Stock Method (Details) - shares
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Earnings per Share        
Securities outstanding included in the computation - Stock options, SARs, and RSUs to purchase common stock 818,574 1,972,905 1,036,051 1,851,419
v3.23.3
Earnings per Share - Summary of Antidilutive Securities Excluded from Computation of Earnings Per Share (Details) - shares
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Stock options, SARs, and RSUs to purchase common stock        
Antidilutive Securities Excluded From Computation Of Earnings Per Share [Line Items]        
Total 5,518,309 4,754,958 5,300,832 4,876,444
v3.23.3
Income Taxes - Schedule of Difference Between Statutory Federal Income Tax Rate (Details)
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Income Taxes        
Federal income tax rate 21.00% 21.00% 21.00% 21.00%
Stock-based compensation   (17.00%) (0.90%) 4.40%
State taxes 4.00% (22.10%) 4.70% (0.50%)
Credits 0.20%   (1.60%) (0.20%)
Other 0.60%   0.30% 0.70%
Valuation allowance   (985.70%)   (144.90%)
Total 25.80% (1003.80%) 23.50% (119.50%)
v3.23.3
Related-party Transactions (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Dec. 31, 2022
Related-party Transactions          
General and administrative $ 22,546 $ 21,331 $ 67,417 $ 61,374  
Amounts due to related parties $ 0   $ 0   $ 0
Other Liability, Related Party, Type [Extensible Enumeration] Related party   Related party   Related party
Amounts due from related parties $ 0   $ 0   $ 0
Other Receivable, after Allowance for Credit Loss, Related Party, Type [Extensible Enumeration] Related party   Related party   Related party
Related party          
Related-party Transactions          
General and administrative $ 73 $ 71 $ 218 $ 213  
v3.23.3
Subsequent Events (Details) - Subsequent Events.
$ / shares in Units, $ in Thousands
Oct. 10, 2023
USD ($)
Right
$ / shares
Oct. 27, 2023
USD ($)
October 2023 Repurchase Program    
Subsequent Event [Line Items]    
Repurchase of shares of common stock approved | $   $ 200,000
Zynerba Pharmaceuticals, Inc.    
Subsequent Event [Line Items]    
Cash consideration per Common Stock | $ / shares $ 1.1059  
Number of contingent value right per Common Stock for each share holder | Right 1  
Contingent consideration per Common Stock | $ / shares $ 2.5444  
Aggregate consideration paid | $ $ 60,000  
v3.23.3
Pay vs Performance Disclosure - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Sep. 30, 2023
Sep. 30, 2022
Sep. 30, 2023
Sep. 30, 2022
Pay vs Performance Disclosure        
Net Income (Loss) $ 38,461 $ 87,943 $ 102,246 $ 132,959
v3.23.3
Insider Trading Arrangements
3 Months Ended
Sep. 30, 2023
Trading Arrangements, by Individual  
Rule 10b5-1 Arrangement Adopted false
Non-Rule 10b5-1 Arrangement Adopted false
Rule 10b5-1 Arrangement Terminated false
Non-Rule 10b5-1 Arrangement Terminated false

Harmony Biosciences (NASDAQ:HRMY)
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Harmony Biosciences (NASDAQ:HRMY)
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