Ovid Therapeutics Reports First Quarter 2022 Financial Results and Corporate Highlights
10 5월 2022 - 9:00PM
Ovid Therapeutics Inc. (NASDAQ: OVID), a biopharmaceutical company
committed to developing medicines designed to conquer epilepsies
and meaningfully improve the lives of people affected by brain
disorders, today reported financial results and corporate
highlights for the first quarter ended March 31, 2022.
“Ovid is focused on propelling our pipeline of
potential medicines with novel mechanisms of action for epilepsies
and seizures,” said Jeremy M. Levin, D. Phil, MB BChir, Chairman
and Chief Executive Officer of Ovid. “We are on track to submit an
IND for OV329, a novel GABA aminotransferase inhibitor, for the
treatment of epilepsies this year. With our strong balance sheet
and experienced team, we believe we have the resources, focus and
knowledge to drive our current programs forward and potentially
augment them with additional candidates and technologies through
business development."
2022 Corporate Highlights &
Anticipated Milestones
- Ovid
expects to file an IND for OV329 and initiate Phase 1 trials in the
fourth quarter of 2022. OV329 is a potent GABA
aminotransferase inhibitor being studied for the treatment of rare
and treatment-resistant forms of epilepsy and seizures, such as
tuberous sclerosis complex, infantile spasms and focal
seizures.
- Data
supporting the preclinical efficacy and safety profile of OV329 are
expected to be presented at epilepsy research meetings in the
second quarter of 2022. Ovid intends to present
preclinical data on OV329 at the EILAT XVI Conference on New
Antiepileptic Drugs and Devices in May and the Epilepsy Foundation
Pipeline Conference in June.
- Ovid
announced its focus on the therapeutic area of epilepsy.
In March 2022, Ovid reshaped its organizational footprint to align
with its focus on epilepsies and direct its resources on its
internal candidates for seizures as well as those acquired through
business development, such as the library of KCC2 activators it
in-licensed last year. As part of the changes, Meg Alexander was
appointed to a newly created position, Chief Corporate Affairs
Officer from her prior role as Head of Communications. The role
consolidates and unites Ovid's engagement strategy across its key
stakeholders including community engagement, patient advocacy,
investor relations and government affairs.
- The Company
announced its financial strategy and expects its cash and cash
equivalents to support advancement of its current epilepsy programs
into 2025.
- Ovid
entered into an agreement with Tufts University under the direction
of Professor Stephen Moss. Dr. Moss, his lab, and team are
recognized leaders in epilepsy research and will support the
translation and development of Ovid candidates, including OV350,
Ovid's direct KCC2 transporter activator candidate.
- Soticlestat
continues to be evaluated by Takeda in two pivotal Phase 3 trials
for Lennox Gastaut and Dravet syndromes. Ovid out-licensed
soticlestat to Takeda and is eligible to receive regulatory and
commercial milestone payments, as well as royalties on global sales
of soticlestat, if it is approved and commercialized.
First Quarter 2022 Financial
Results
- Cash and cash
equivalents as of March 31, 2022 was $166.7 million.
- Revenue for
the first quarter ended March 31, 2022 was $1.4 million, as
compared to $208.4 million for the same period in 2021. Revenue
recognized for the first quarter ended March 31, 2022 was
associated with licensing transactions with Marinus
Pharmaceuticals, Inc. and Healx, Ltd. Revenue recognized for the
first quarter ended March 31, 2021 was associated with licensing
transactions with Takeda Pharmaceuticals (Takeda) and Angelini
Pharma, Inc. (Angelini Pharma).
- Research and
development expenses were $7.8 million for the quarter ended
March 31, 2022, as compared to $16.2 million for the same
period in 2021. The decrease of $8.4 million was primarily due to
the decision to discontinue the clinical study of OV101 in Angelman
syndrome and Fragile X syndrome, and the termination of the Takeda
Collaboration Agreement for OV935. The decrease was offset by a
payroll and payroll-related expense increase of $1.0 million, which
was primarily related to severance pay recognized during the
period.
- General and
administrative expenses were $9.9 million for the quarter ended
March 31, 2022, as compared to $15.6 million for the same
period. Expenses decreased by $5.7 million. This was primarily due
to a $7.2 million decrease in legal, professional, and advisory
fees that were related to the execution of the Takeda License and
Termination Agreement. Partially offsetting these decreases were
payroll and payroll-related expenses, which increased by $1.0
million, and were primarily related to severance pay recognized
during the period.
- The Company
reported net loss of approximately $16.1 million, or basic and
diluted net loss per share attributable to common stockholders of
$0.23 for the quarter ended March 31, 2022. Net income was $176.0
million for the same period in 2021, resulting in basic net income
per share of $2.55 and diluted net income per share of $2.53. Net
income for the three months ended March 31, 2021, was
attributable to a one-time upfront payment of $196.0 million
(pre-tax) pursuant to the Takeda License and Termination Agreement,
and $12.4 million recognized in connection with the termination of
the license and collaboration agreement with Angelini Pharma.
- Operating
expenses were $17.7 million for the quarter ended March 31,
2022, and non-GAAP adjusted operating expenses (which exclude
non-recurring expenses and non-cash expenses; see table on
Reconciliation of Non-GAAP Expenses) were $14.2 million for the
quarter. See “Non-GAAP Financial Measures” below for a discussion
of non-GAAP adjusted operating expenses.
Non-GAAP Financial Measures
This press release presents non-GAAP adjusted
operating expenses on a historical and projected basis. For the
period presented, non-GAAP adjusted operating expenses exclude from
operating expenses, as calculated and presented in accordance with
GAAP, the following non-recurring, non-cash and non-routine items:
wind down of OV101 clinical costs; stock-based compensation, and
severance fees. Non-GAAP adjusted operating expenses is a financial
measure that has not been prepared in accordance with GAAP.
Accordingly, investors should consider non-GAAP adjusted operating
expenses in addition to, but not as a substitute for, operating
expenses that we calculate and present in accordance with GAAP.
Among other things, our management uses non-GAAP adjusted operating
expenses to establish budgets and operational goals and to manage
our business. Other companies may define or use this measure in
different ways. We believe that the presentation of non-GAAP
adjusted operating expenses provides investors and management with
helpful supplemental information relating to operating performance
and trends. A table reconciling non-GAAP adjusted operating
expenses to operating expenses for all historical periods presented
is included below under the heading “Reconciliation of Non-GAAP
Adjusted Operating Expenses to Operating Expenses.”
About Ovid Therapeutics
Ovid Therapeutics Inc. is a New York-based
biopharmaceutical company striving to conquer seizures and brain
disorders with courageous science. Ovid’s pipeline of small
molecule and genetic medicines candidates seek to meaningfully
improve the lives of people and families affected by epilepsies.
Ovid is developing OV329, a GABA aminotransferase inhibitor, for
treatment-resistant seizures; and OV350, a direct activator of the
KCC2 transporter, for potential treatment of epilepsies. In
addition, Ovid maintains a significant financial interest in the
future regulatory development and potential commercialization of
soticlestat, which Takeda is responsible for advancing globally.
Soticlestat is a cholesterol 24 hydroxylase inhibitor, which is
currently in Phase 3 trials for Dravet and Lennox-Gastaut
syndromes. For more information about these and other Ovid research
programs, please visit www.ovidrx.com.
Forward-Looking Statements
This press release includes certain disclosures
that contain “forward-looking statements,” including, without
limitation, statements regarding the timing and development of
Ovid’s product candidate pipeline and achievement of expected near-
and long-term milestones, including the filing of an IND for and
anticipated timing of clinical trials of OV329, Ovid’s business
development intentions, the ability of Dr. Moss’s team and lab to
support the translation and development of Ovid candidates under
the research agreement with Tufts University, the potential
therapeutic benefits of Ovid’s current or future product
candidates, the continued development of soticlestat by Takeda, the
clinical and regulatory development and potential commercialization
of soticlestat, OV329, OV350, or any of Ovid’s other current or
future product candidates, and Ovid’s expectations regarding its
cash runway. You can identify forward-looking statements because
they contain words such as “will,” “believes,” “intends,”
“anticipates” and “expects.” Forward-looking statements are based
on Ovid’s current expectations and assumptions. Because
forward-looking statements relate to the future, they are subject
to inherent uncertainties, risks and changes in circumstances that
may differ materially from those contemplated by the
forward-looking statements, which are neither statements of
historical fact nor guarantees or assurances of future performance.
Important factors that could cause actual results to differ
materially from those in the forward-looking statements include,
without limitation, uncertainties inherent in the preclinical and
clinical development and regulatory approval processes, risks
related to Ovid’s ability to achieve its financial objectives, the
risk that Ovid may not be able to realize the intended benefits of
its technology or its business strategy, risks related to Ovid’s
ability to identify business development targets or strategic
partners, to enter into strategic transactions on favorable terms,
or to consummate and realize the benefits of any business
development transactions and risks to Ovid’s or any of its
partners’ abilities to meet anticipated deadlines and milestones
presented by the ongoing COVID-19 pandemic. Additional risks that
could cause actual results to differ materially from those in the
forward-looking statements are set forth under the caption “Risk
Factors” in Ovid’s Annual Report on Form 10-K filed with the
Securities and Exchange Commission (SEC) on March 15, 2022, and in
future filings Ovid makes with the SEC. Any forward-looking
statements contained in this press release speak only as of the
date hereof, and Ovid assumes no obligation to update any
forward-looking statements contained herein, whether because of any
new information, future events, changed circumstances or otherwise,
except as otherwise required by law.
Condensed Consolidated Statements of
OperationsUnaudited
|
For The Three MonthsEnded March 31,2022 |
|
|
For The Three MonthsEnded March 31,2021 |
|
Revenue: |
|
|
|
|
|
License and other revenue |
$ |
1,445,366 |
|
|
$ |
12,382,779 |
|
License revenue - related party |
|
- |
|
|
|
196,000,000 |
|
Total revenue |
|
1,445,366 |
|
|
|
208,382,779 |
|
Operating expenses: |
|
|
|
|
|
Research and development |
$ |
7,832,269 |
|
|
$ |
16,248,909 |
|
General and administrative |
|
9,880,203 |
|
|
|
15,576,554 |
|
Total operating expenses |
|
17,712,472 |
|
|
|
31,825,463 |
|
(Loss) income from
operations |
|
(16,267,107 |
) |
|
|
176,557,316 |
|
Other income (expenses),
net |
|
209,050 |
|
|
|
(49,732 |
) |
(Loss) income before provision
for income taxes |
|
(16,058,056 |
) |
|
|
176,507,584 |
|
Provision for income
taxes |
|
50,000 |
|
|
|
500,277 |
|
Net (loss) income |
$ |
(16,108,056 |
) |
|
$ |
176,007,307 |
|
Net (loss) income per share,
basic |
$ |
(0.23 |
) |
|
$ |
2.55 |
|
Net (loss) income per share,
diluted |
$ |
(0.23 |
) |
|
$ |
2.53 |
|
Weighted-average common shares
outstanding, basic |
|
70,345,828 |
|
|
|
66,088,592 |
|
Weighted-average common shares
outstanding, diluted |
|
70,345,828 |
|
|
|
66,578,377 |
|
Select Condensed Balance Sheet
DataUnaudited
|
March 31,2022 |
|
|
December 31,2021 |
|
|
|
|
|
|
|
Cash and cash equivalents |
$ |
166,668,027 |
|
|
$ |
187,797,532 |
|
Working capital1 |
|
159,859,469 |
|
|
|
175,680,808 |
|
Total assets |
|
191,096,074 |
|
|
|
194,544,757 |
|
Total stockholder's equity |
|
164,996,271 |
|
|
|
179,746,436 |
|
|
|
|
|
|
|
1Working capital defined as
current assets less current liabilities |
|
|
|
|
|
Reconciliation of Non-GAAP Adjusted
Operating Expenses to Operating Expenses
|
Three MonthsEnded March 31,2022 |
|
|
Three MonthsEnded March 31,2021 |
|
|
|
|
|
|
|
Operating expenses |
$ |
17,712,472 |
|
|
$ |
31,825,463 |
|
|
|
|
|
|
|
Non-recurring and non-cash
items included therein: |
|
|
|
|
|
Stock-based compensation |
|
1,324,812 |
|
|
|
1,320,002 |
|
Severance pay |
|
1,978,286 |
|
|
|
- |
|
Wind-down of OV101 clinical costs |
|
243,187 |
|
|
|
3,750,280 |
|
|
|
|
|
|
|
Non-GAAP adjusted operating
expenses |
$ |
14,166,188 |
|
|
$ |
26,755,181 |
|
Contacts
Investors and Media:Ovid
Therapeutics Inc.Meg Alexander917-943-6681malexander@ovidrx.com
OR
Investors:Argot PartnersDawn
Schottlandt212-600-1902ovid@argotpartners.com
Ovid Therapeutics (NASDAQ:OVID)
과거 데이터 주식 차트
부터 1월(1) 2025 으로 2월(2) 2025
Ovid Therapeutics (NASDAQ:OVID)
과거 데이터 주식 차트
부터 2월(2) 2024 으로 2월(2) 2025