SECURITIES AND EXCHANGE COMMISSION
Washington, D.C.  20549
 
FORM 8-K
 
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
 
Date of report (Date of earliest event reported):  November 6, 2024
 
IONIS PHARMACEUTICALS, INC.
(Exact Name of Registrant as Specified in Charter)
 
Delaware
(State or Other Jurisdiction of Incorporation)
 
000-19125
 
33-0336973
(Commission File No.)
 
(IRS Employer Identification No.)

2855 Gazelle Court
Carlsbad, CA 92010
(Address of Principal Executive Offices and Zip Code)
 
Registrant’s telephone number, including area code: (760) 931-9200


Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:


Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)


Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)


Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))


Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
 
Securities registered pursuant to Section 12(b) of the Act:

Title of each class
 
Trading symbol
 
Name of each exchange on which registered
Common Stock, $.001 Par Value
 
IONS
 
The Nasdaq Stock Market, LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (Section 230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (Section 240.12b-2 of this chapter).

   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.     ☐
 


Item 2.02
Results of Operations and Financial Condition.
 
On November 6, 2024, Ionis Pharmaceuticals, Inc. (the “Company”) issued a press release announcing the Company’s financial results for the quarter ended September 30, 2024.  In addition to disclosing results that are determined in accordance with Generally Accepted Accounting Principles (“GAAP”), the Company also discloses pro forma or non-GAAP results of operations, which are adjusted from GAAP to exclude non-cash compensation expense related to equity awards and the related tax effects. The Company is presenting pro forma information excluding non-cash compensation expense and the related tax effects because the Company believes it better enables financial statement users to assess and compare its historical performance and project its future operating results and cash flows.  A copy of the release is furnished with this report as an exhibit pursuant to “Item 2.02. Results of Operations and Financial Condition” of Form 8-K in accordance with SEC Release Nos. 33-8216 and 34-47583.
 
The information in this Current Report on Form 8-K and the Exhibit attached hereto shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, regardless of any general incorporation language in such filing.
 
Item 9.01.
Financial Statements and Exhibits.
 
(d) Exhibits.
 
Exhibit No.
Description
Press Release dated November 6, 2024.
   
 104
Cover Page Interactive Data File (embedded within the Inline XBRL document).


SIGNATURE
 
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
 
 
Ionis Pharmaceuticals, Inc.
     
Dated:  November 6, 2024
By:
/s/ Patrick R. O’Neil
   
Patrick R. O’Neil
   
Executive Vice President, Chief Legal Officer and General Counsel




Exhibit 99.1


Ionis reports third quarter 2024 financial results

WAINUATM U.S. launch progressing well; approved in UK; positive CHMP opinion
 
Olezarsen FCS PDUFA December 19, 2024
 
Donidalorsen HAE PDUFA August 21, 2025; EU regulatory submission in process
 
On track to achieve 2024 P&L financial guidance; increased 2024 cash guidance
 
CARLSBAD, Calif., November 6, 2024 – Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) (the “Company”) today reported financial results for the third quarter of 2024.
 
“Today, we stand on the cusp of a new era for Ionis, with our first co-commercialization launch proceeding well with WAINUA, our first planned independent launch fast approaching and continued strong progress across our rich pipeline. With an upcoming December FDA action date, we are ready to independently bring olezarsen to people with familial chylomicronemia syndrome, a serious rare disease with no approved treatments in the U.S. We are similarly well positioned for our second independent launch for donidalorsen, which we believe could become a preferred treatment choice for people with hereditary angioedema, with an FDA action date of August 21, 2025,” said Brett P. Monia, Ph.D., chief executive officer of Ionis. “In parallel, we are making great progress across the rest of our rich Phase 3 pipeline. We expect Phase 3 results supporting olezarsen’s second indication in severe hypertriglyceridemia and pelacarsen in Lp(a)-driven cardiovascular disease next year, as well as Phase 3 results supporting eplontersen’s second indication in ATTR cardiomyopathy in the second half of 2026. We are also advancing our next wave of potentially transformational wholly owned medicines, including ION582 for Angelman syndrome, which we expect to enter Phase 3 development in the first half of next year following our positive end of Phase 2 discussion with the FDA. Our recent achievements, together with our advancing and expanding pipeline, position Ionis to deliver on our goal to bring a steady cadence of transformational medicines to people with serious diseases.”
 
Third Quarter 2024 Summary Financial Results(1):

   
Three months
ended
September 30,
   
Nine months
ended
September 30,
 
   
2024
   
2023
   
2024
   
2023
 
   
(amounts in millions)
 
Total revenue
 
$
134
   
$
144
   
$
479
   
$
463
 
Operating expenses
 
$
282
   
$
287
   
$
843
   
$
811
 
Operating expenses on a non-GAAP basis
 
$
250
   
$
261
   
$
749
   
$
732
 
Loss from operations
 
(148
)
 
(143
)
 
(364
)
 
(348
)
Loss from operations on a non-GAAP basis
 
(116
)
 
(117
)
 
(270
)
 
(269
)

  (1)
Reconciliation of GAAP to non-GAAP basis contained later in this release.

1

Financial Highlights
 
Revenue for the three and nine months ended September 30, 2024 decreased by 7% and increased by 3% compared to the same periods last year, respectively. Ionis continued to generate revenue from diverse sources, including a new source of royalty revenue with the launch of WAINUA in the U.S in the first quarter
 
Operating expenses for the three and nine months ended September 30, 2024 increased as planned compared to the same periods last year, excluding certain one-time costs in 2023, reflecting continued investments in late-stage development, including WAINUA for ATTR cardiomyopathy (ATTR-CM) and olezarsen for severe hypertriglyceridemia (sHTG), and commercialization efforts for WAINUA, olezarsen and donidalorsen
 
Reaffirmed 2024 P&L financial guidance, increased cash guidance to $2.2 billion reflecting proceeds from equity offering

Recent Marketed Medicines Highlights
 
WAINUA (WAINZUA in Europe) for the treatment of adults with polyneuropathy of hereditary transthyretin-mediated amyloidosis (ATTRv-PN) achieved multiple commercial and regulatory milestones:
 

o
Generated sales of $23 million and $44 million resulting in royalty revenue of $5 million and $10 million in the three and nine months ended September 30, 2024, respectively
 

o
Received positive Committee for Medicinal Products for Human Use (CHMP) opinion from European Medicines Agency (EMA) for the treatment of hereditary transthyretin-mediated amyloidosis in adult patients with stage 1 or stage 2 polyneuropathy
 

o
Approved in UK by the Medicines and Healthcare products Regulatory Agency (MHRA) with an accelerated National Institute for Health and Care Excellence (NICE) recommendation; earning $30 million from AstraZeneca
 

o
Launch underway in Canada, following approval and reimbursement from Health Canada
 
SPINRAZA® (nusinersen) for the treatment of spinal muscular atrophy (SMA) generated global sales of $381 million and $1.2 billion resulting in royalty revenue of $57 million and $152 million in the three and nine months ended September 30, 2024, respectively
 

o
Positive Phase 2/3 DEVOTE study data presented from higher dose nusinersen; global regulatory applications planned
 
QALSODY® (tofersen) granted marketing approval in China for the treatment of SOD1-ALS

Recent Late-Stage Pipeline Highlights

Olezarsen positioned to potentially treat two patient populations with urgent unmet need, familial chylomicronemia syndrome (FCS) and severe hypertriglyceridemia (sHTG):
 

o
NDA for patients with FCS under FDA Priority Review with a PDUFA date of December 19, 2024
 

o
Marketing authorization application (MAA) under regulatory review by the EMA
 

o
Ongoing pivotal development program for sHTG on track for data in H2:2025
 
Donidalorsen Phase 3 data position it to potentially launch next year as the first RNA-targeted prophylactic treatment for people with hereditary angioedema (HAE):

2


o
FDA accepted the NDA for patients with HAE with a PDUFA date of August 21, 2025; Otsuka, Europe and Asia Pacific partner, preparing to submit MAA
 

o
Presented positive Phase 2 open label extension (OLE) study data in patients treated up to three years with every four weeks or every eight weeks dosing
 
Zilganersen Phase 3 study fully enrolled as a potential treatment for Alexander disease; on track for data in 2025
 

o
Granted Fast Track designation by the FDA
 
ION582 achieved important clinical and regulatory milestones enabling initiation of Phase 3 development in Angelman syndrome (AS) in H1:2025:
 

o
Presented positive Phase 1/2 data in patients with AS at Angelman Syndrome Foundation (ASF) Family Conference
 

o
Completed positive End-of-Phase 2 discussion with FDA, included alignment on Phase 3 design
 
Reported positive data from the Phase 2 study of IONIS-FB-LRx in patients with immunoglobulin A nephropathy (IgAN); Roche continues to advance IONIS-FB-LRx in the Phase 3 IMAGINATION study
 
Recent Other Pipeline Updates

Sapablursen for the treatment of polycythemia vera granted orphan drug designation by FDA; enrollment complete in Phase 2 IMPRSSION study with data expected in 2025

IONIS-MAPTRx (BIIB080) enrollment complete in Phase 2 CELIA study in patients with early Alzheimer’s disease (AD); data expected in 2026
 
Initiated first in human studies with multiple medicines from neurological disease pipeline:
 

o
Phase 1/2 Orbit study of ION356 (PLP1) in patients with Pelizaeus-Merzbacher disease (PMD)
 

o
Phase 1/2 HERO study of ION269 (APP), for the potential treatment of Alzheimer’s disease (AD), which is initially being evaluated in patients with Down syndrome (DS) who have a genetic risk for developing AD
 

o
Phase 1/2 ATTUNE study of ION440 (MECP2) in patients with MECP2 duplication syndrome

Third Quarter 2024 Financial Results
 
“This year has been marked by strong delivery on our pipeline and business goals, which position Ionis to deliver on our vision of bringing a steady cadence of innovative medicines to patients in need. Fully realizing these significant opportunities requires substantial investment. As a result, we recently executed an equity offering that extends our cash runway, enabling us to continue to invest in the numerous attractive opportunities ahead of us, including our near-term commercial launches with multi-billion-dollar revenue potential and our rich late and mid-stage pipeline,” said Elizabeth L. Hougen, chief financial officer of Ionis. “Looking beyond this year, we will continue to invest in go-to-market preparations for our planned olezarsen and donidalorsen launches. Additionally, with our increased confidence in the potential of WAINUA and olezarsen to address broader patient populations, we plan to scale our capabilities in line with the significant potential of these important medicines. At the same time, we are investing in our next wave of medicines, including pre-commercialization activities and Phase 3 development for ION582 for Angelman syndrome and zilganersen for Alexander disease. We expect our investments today will position Ionis for sustainable growth for years to come.

3

Revenue

Ionis’ revenue was comprised of the following:

   
Three months ended
   
Nine months ended
 
   
September 30,
   
September 30,
 
   
2024
   
2023
   
2024
   
2023
 
Revenue:
 
(amounts in millions)
 
Commercial revenue:
                       
SPINRAZA royalties
 
$
57
   
$
67
   
$
152
   
$
179
 
WAINUA royalties
   
5
     
-
     
10
     
-
 
Other commercial revenue:
                               
TEGSEDI and WAYLIVRA revenue, net
   
9
     
8
     
26
     
25
 
Licensing and other royalty revenue
   
5
     
9
     
19
     
26
 
Total commercial revenue
   
76
     
84
     
207
     
230
 
Research and development revenue:
                               
Amortization from upfront payments
   
28
     
18
     
105
     
47
 
Milestone payments
   
16
     
16
     
76
     
90
 
License fees
   
-
     
5
     
38
     
25
 
Other services
   
1
     
5
     
18
     
11
 
Collaborative agreement revenue
   
45
     
44
     
237
     
173
 
WAINUA joint development revenue
   
13
     
16
     
35
     
60
 
Total research and development revenue
   
58
     
60
     
272
     
233
 
Total revenue
 
$
134
   
$
144
   
$
479
   
$
463
 

Commercial revenue for the three and nine months ended September 30, 2024 included a new source of royalty revenue with the launch of WAINUA in the U.S. in late January 2024. Ionis’ commercial revenue for the three and nine months ended September 30, 2024 and 2023 also included royalties from the net sales of QALSODY, which Biogen launched in the U.S. in the second quarter of 2023 and in the EU in the second quarter of 2024. SPINRAZA product sales for the three months ended September 30, 2024 compared to the same period last year increased slightly in the U.S. and decreased outside of the U.S. primarily due to an annual order from a single country that did not recur in 2024.

R&D revenue was relatively consistent for the three months ended September 30, 2024 compared to the same period last year. R&D revenue increased for the nine months ended September 30, 2024 compared to the same period last year primarily due to the amortization of upfront payments from the new collaborations with Roche and Novartis that Ionis entered into during the second half of last year. In addition, license fees increased year over year as a result of new collaborations Ionis entered into during the second quarter of 2024, including the expanded donidalorsen licensing agreement with Otsuka, which now includes the Asia-Pacific region in addition to Europe. These increases were partially offset by the decrease in WAINUA joint development revenue, which decreased as development activities relating to ATTRv-PN wound down with the launch of WAINUA for this indication.

4

Operating Expenses
 
Ionis’ operating expenses, excluding one-time costs associated with a lease exit in the third quarter of 2023, increased for the three and nine months ended September 30, 2024 compared to the same periods in 2023, consistent with expectations. SG&A expenses increased year over year primarily due to the launch of WAINUA in the U.S. and launch preparation activities for olezarsen and donidalorsen, including establishing the field team for olezarsen in the second quarter of 2024. R&D expenses were essentially flat for the three and nine months ended September 30, 2024 compared to the same periods last year as several late-stage studies have ended.

Balance Sheet

As of September 30, 2024, Ionis’ cash, cash equivalents and short-term investments increased to $2.5 billion compared to $2.3 billion at December 31, 2023. In September 2024, Ionis issued 11.5 million shares of its common stock at a public offering price of $43.50 per share that generated gross proceeds of $500 million, before deducting underwriting discounts and commissions and other offering expenses payable by Ionis. The Company plans to continue deploying its capital resources toward growth opportunities, and projects to end 2024 with $2.2 billion in cash, cash equivalents and short-term investments. Ionis’ working capital also increased over the same period primarily due to the Company’s higher cash and short-term investments balance. As a result of Ionis’ advancing pipeline that has delivered several positive data readouts, Ionis expects to make increased investments in the years ahead with the goal to realize the value of these opportunities, with a focus on its wholly owned late-stage and next wave of innovative medicines.

Webcast

Management will host a conference call and webcast to discuss Ionis’ third quarter 2024 results at 11:30 a.m. Eastern time on Wednesday, November 6, 2024. Interested parties may access the webcast here. A webcast replay will be available for a limited time at the same address. To access the Company’s third quarter 2024 earnings slides click here.

For more information about SPINRAZA and QALSODY, visit https://www.spinraza.com/ and https://www.qalsody.com/, respectively. QALSODY is approved under accelerated approval based on reduction in plasma neurofilament light chain (NfL) observed in patients treated with QALSODY. Continued approval may be contingent upon verification of clinical benefit in confirmatory trial(s).

INDICATION for WAINUA™ (eplontersen)
WAINUA injection, for subcutaneous use, 45 mg is indicated for the treatment of the polyneuropathy of hereditary transthyretin-mediated amyloidosis in adults.

IMPORTANT SAFETY INFORMATION for WAINUA™ (eplontersen)

WARNINGS AND PRECAUTIONS
Reduced Serum Vitamin A Levels and Recommended Supplementation WAINUA leads to a decrease in serum vitamin A levels. Supplement with recommended daily allowance of vitamin A. Refer patient to an ophthalmologist if ocular symptoms suggestive of vitamin A deficiency occur.

ADVERSE REACTIONS
Most common adverse reactions (≥9% in WAINUA-treated patients) were vitamin A decreased (15%) and vomiting (9%).

Please see link to U.S. Full Prescribing Information for WAINUA.

5

About Ionis Pharmaceuticals, Inc.
 
For three decades, Ionis has invented medicines that bring better futures to people with serious diseases. Ionis currently has five marketed medicines and a leading pipeline in neurology, cardiology, and other areas of high patient need. As the pioneer in RNA-targeted medicines, Ionis continues to drive innovation in RNA therapies in addition to advancing new approaches in gene editing. A deep understanding of disease biology and industry-leading technology propels our work, coupled with a passion and urgency to deliver life-changing advances for patients. To learn more about Ionis, visit Ionis.com and follow us on X (Twitter), LinkedIn and Instagram.

Ionis’ Forward-looking Statement
 
This press release includes forward-looking statements regarding Ionis’ business, financial guidance and the therapeutic and commercial potential of our commercial medicines, additional medicines in development and technologies. Any statement describing Ionis’ goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be considered an at-risk statement. Such statements are subject to certain risks and uncertainties including those inherent in the process of discovering, developing and commercializing medicines that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such medicines. Ionis’ forward-looking statements also involve assumptions that, if they never materialize or prove correct, could cause its results to differ materially from those expressed or implied by such forward-looking statements. Although Ionis’ forward-looking statements reflect the good faith judgment of its management, these statements are based only on facts and factors currently known by Ionis. Except as required by law, we undertake no obligation to update any forward-looking statements for any reason. As a result, you are cautioned not to rely on these forward-looking statements. These and other risks concerning Ionis' programs are described in additional detail in Ionis' annual report on Form 10-K for the year ended December 31, 2023, and most recent Form 10-Q, which are on file with the Securities and Exchange Commission. Copies of these and other documents are available from the Company.

In this press release, unless the context requires otherwise, “Ionis,” “Company,” “we,” “our” and “us” all refer to Ionis Pharmaceuticals and its subsidiaries.

Ionis Pharmaceuticals® is a registered trademark of Ionis Pharmaceuticals, Inc. Akcea Therapeutics® is a registered trademark of Akcea Therapeutics, Inc. TEGSEDI® is a registered trademark of Akcea Therapeutics, Inc. WAYLIVRA® is a registered trademark of Akcea Therapeutics, Inc. SPINRAZA® and QALSODY® are registered trademarks of Biogen. WAINUATM is a registered trademark of the AstraZeneca group of companies.

Ionis Investor Contact:
D. Wade Walke, Ph.D.
IR@ionis.com
760-603-2331

Ionis Media Contact:
Hayley Soffer
media@ionis.com
760-603-4679

6

IONIS PHARMACEUTICALS, INC.
SELECTED FINANCIAL INFORMATION
Condensed Consolidated Statements of Operations
(In Millions, Except Per Share Data)

   
Three months ended
   
Nine months ended
 
   
September 30,
   
September 30,
 
   
2024
   
2023
   
2024
   
2023
 
   
(unaudited)
 
Revenue:
                       
Commercial revenue:
                       
SPINRAZA royalties
 
$
57
   
$
67
   
$
152
   
$
179
 
WAINUA royalties
   
5
     
-
     
10
     
-
 
Other commercial revenue
   
14
     
17
     
45
     
51
 
Total commercial revenue
   
76
     
84
     
207
     
230
 
Research and development revenue:
                               
Collaborative agreement revenue
   
45
     
44
     
237
     
173
 
WAINUA joint development revenue
   
13
     
16
     
35
     
60
 
Total research and development revenue
   
58
     
60
     
272
     
233
 
Total revenue
   
134
     
144
     
479
     
463
 
Expenses:
                               
Cost of sales
   
1
     
2
     
7
     
6
 
Research, development and patent
   
220
     
215
     
656
     
643
 
Selling, general and administrative
   
61
     
70
     
180
     
162
 
Total operating expenses
   
282
     
287
     
843
     
811
 
Loss from operations
   
(148
)
   
(143
)
   
(364
)
   
(348
)
                                 
Other income (expense):
                               
Interest expense related to the sale of future royalties
   
(19
)
   
(18
)
   
(55
)
   
(51
)
Other income, net
   
23
     
20
     
66
     
68
 
Loss before income tax benefit (expense)
   
(144
)
   
(141
)
   
(353
)
   
(331
)
                                 
Income tax benefit (expense)
   
4
     
(6
)
   
3
     
(26
)

                               
Net loss
 
(140
)
 
(147
)
 
(350
)
 
(357
)
                                 
Basic and diluted net loss per share
 
(0.95
)
 
(1.03
)
 
(2.38
)
 
(2.50
)
Shares used in computing basic and diluted net loss per share
   
149
     
143
     
147
     
143
 

7

IONIS PHARMACEUTICALS, INC.
Reconciliation of GAAP to Non-GAAP Basis:
Condensed Consolidated Operating Expenses, Loss From Operations, and Net Loss
(In Millions)

   
Three months ended
September 30,
   
Nine months ended
September 30,
 
   
2024
   
2023
   
2024
   
2023
 
   
(unaudited)
 
As reported research, development and patent expenses according to GAAP
 
$
220
   
$
215
   
$
656
   
$
643
 
Excluding compensation expense related to equity awards
   
(22
)
   
(19
)
   
(67
)
   
(58
)
Non-GAAP research, development and patent expenses
 
$
198
   
$
196
   
$
589
   
$
585
 
                                 
As reported selling, general and administrative expenses according to GAAP
 
$
61
   
$
70
   
$
180
   
$
162
 
Excluding compensation expense related to equity awards
   
(10
)
   
(7
)
   
(26
)
   
(22
)
Non-GAAP selling, general and administrative expenses
 
$
51
   
$
63
   
$
154
   
$
140
 
                                 
As reported operating expenses according to GAAP
 
$
282
   
$
287
   
$
843
   
$
811
 
Excluding compensation expense related to equity awards
   
(32
)
   
(26
)
   
(94
)
   
(79
)
Non-GAAP operating expenses
 
$
250
   
$
261
   
$
749
   
$
732
 
                                 
As reported loss from operations according to GAAP
 
(148
)
 
(143
)
 
(364
)
 
(348
)
Excluding compensation expense related to equity awards
   
(32
)
   
(26
)
   
(94
)
   
(79
)
Non-GAAP loss from operations
 
(116
)
 
(117
)
 
(270
)
 
(269
)
                                 
As reported net loss according to GAAP
 
(140
)
 
(147
)
 
(350
)
 
(357
)
Excluding compensation expense related to equity awards and related tax effects
   
(32
)
   
(26
)
   
(94
)
   
(79
)
Non-GAAP net loss
 
(108
)
 
(121
)
 
(256
)
 
(278
)

Reconciliation of GAAP to Non-GAAP Basis
 
As illustrated in the Selected Financial Information in this press release, non-GAAP operating expenses, non-GAAP loss from operations, and non-GAAP net loss were adjusted from GAAP to exclude compensation expense related to equity awards and the related tax effects. Compensation expense related to equity awards are non-cash. These measures are provided as supplementary information and are not a substitute for financial measures calculated in accordance with GAAP. Ionis reports these non-GAAP results to better enable financial statement users to assess and compare its historical performance and project its future operating results and cash flows. Further, the presentation of Ionis’ non-GAAP results is consistent with how Ionis’ management internally evaluates the performance of its operations.
 
8

IONIS PHARMACEUTICALS, INC.
Condensed Consolidated Balance Sheets
(In Millions)
 
   
September 30,
   
December 31,
 
   
2024
   
2023
 
   
(unaudited)
       
Assets:
           
Cash, cash equivalents and short-term investments
 
$
2,483
   
$
2,331
 
Contracts receivable
   
18
     
98
 
Other current assets
   
213
     
213
 
Property, plant and equipment, net
   
83
     
71
 
Right-of-use assets
   
164
     
172
 
Other assets
   
120
     
105
 
Total assets
 
$
3,081
   
$
2,990
 
                 
Liabilities and stockholders’ equity:
               
Current portion of deferred contract revenue
 
$
76
   
$
151
 
0.125% convertible senior notes, net – short-term
   
44
     
44
 
Other current liabilities
   
184
     
253
 
1.75% convertible senior notes, net
   
564
     
562
 
0% convertible senior notes, net
   
628
     
625
 
Liability related to sale of future royalties, net
   
538
     
514
 
Long-term lease liabilities
   
168
     
171
 
Long-term obligations, less current portion
   
43
     
42
 
Long-term deferred contract revenue
   
174
     
241
 
Total stockholders’ equity
   
662
     
387
 
Total liabilities and stockholders’ equity
 
$
3,081
   
$
2,990
 

9

Key 2024 Value Driving Events(1)
 
 
New Product Launches
 
Program

Indication
Achieved
 
WAINUA

ATTRv-PN
 
Olezarsen

FCS
 
 
QALSODY (EU)

SOD1-ALS


Regulatory Actions
 
Program
 
Indication
 
Regulatory Action
Achieved
 
Eplontersen
 
ATTRv-PN
 
Additional OUS filings
 
EMA approval decision
 
 
Additional OUS approval decision(s)
 
Olezarsen
 
FCS
 
FDA approval decision
 
 
NDA filing
 
EU filing
 
Canada filing
 
 
Donidalorsen
 
HAE
 
NDA filing
 
QALSODY
 
SOD1-ALS
 
EMA approval decision
 
China approval

 
Key Phase 3 Clinical Data Events
 
Program
 
Indication
 
Event
Achieved
 
Olezarsen
 
FCS
 
Balance study full data
 
Donidalorsen
 
HAE
 
OASIS-HAE topline data
 
Donidalorsen
 
HAE
 
OASIS-HAE full data
 
Donidalorsen
 
HAE
 
OASIS-Plus: OLE + Switch data
 
Nusinersen
 
SMA
 
DEVOTE study data (higher dose)


Key Phase 2 Clinical Data Events
 
Program
 
Indication
 
Event
Achieved
 
Donidalorsen
 
HAE
 
3-year Phase 2 OLE data
 
IONIS-FB-LRx
 
IgAN
 
Phase 2 data
 
IONIS-FB-LRx
 
GA
 
GOLDEN study data
--
 
ION224 (DGAT2)
 
NASH
 
Phase 2 data
 
ION582 (UBE3A)
 
Angelman syndrome
 
HALOS study data
 
ION541 (ATXN2)
 
ALS
 
ALSpire study data
--
 
Sapablursen (TMPRSS6)
 
Polycythemia vera
 
IMPRSSION study full enrollment
 
IONIS-MAPTRx (Tau)
 
Alzheimer’s disease
 
CELIA study full enrollment

  (1)
Timing expectations based on current assumptions and subject to change.


Milestone achieved

--     Milestone achieved, however program discontinued
 
#   #   #


10

v3.24.3
Document and Entity Information
Nov. 06, 2024
Cover [Abstract]  
Document Type 8-K
Amendment Flag false
Document Period End Date Nov. 06, 2024
Entity File Number 000-19125
Entity Registrant Name IONIS PHARMACEUTICALS, INC.
Entity Central Index Key 0000874015
Entity Incorporation, State or Country Code DE
Entity Tax Identification Number 33-0336973
Entity Address, Address Line One 2855 Gazelle Court
Entity Address, City or Town Carlsbad
Entity Address, State or Province CA
Entity Address, Postal Zip Code 92010
City Area Code 760
Local Phone Number 931-9200
Title of 12(b) Security Common Stock, $.001 Par Value
Trading Symbol IONS
Security Exchange Name NASDAQ
Entity Emerging Growth Company false
Written Communications false
Soliciting Material false
Pre-commencement Tender Offer false
Pre-commencement Issuer Tender Offer false

Ionis Pharmaceuticals (NASDAQ:IONS)
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Ionis Pharmaceuticals (NASDAQ:IONS)
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