Ovid Therapeutics Inc. (NASDAQ: OVID), a biopharmaceutical company
committed to developing medicines that transform the lives of
people with rare epilepsies and seizure-related disorders, today
announced leadership appointments intended to enhance the execution
of its corporate strategy and the scientific stewardship of its
therapeutic development programs. The Company also announced
changes to its administrative functions intended to enhance
efficiency and reduce costs.
“We are excited as Zhong and Manoj respectively
assume research and development leadership of Ovid’s focused
pipeline of potential first-in-class and best-in-class CNS
programs,” said Jeremy Levin, D. Phil, MB BChir, Chairman and Chief
Executive Officer of Ovid Therapeutics. “Both have successfully
developed many anti-seizure and other CNS medicines. By adding
their collective knowledge, experience, and management skills to
Ovid, we seek to rapidly advance and accelerate our exciting
programs,” remarked Dr. Levin.
Scientific Leadership & Development
Appointments
Dr. Zhong will lead all non-clinical scientific
and research activities that support the advancement of Ovid’s
pipeline of potential therapeutic candidates for the treatment of
epilepsy and seizure-related disorders. In this role, Dr. Zhong
will oversee Ovid’s scientific strategy and the Company’s research
team and academic collaborations with the goal of accelerating
research that underpins the clinical development of: OV329, a
next-generation GABA aminotransferase inhibitor; selective ROCK2
inhibitors for rare neurological conditions, including GV101 for
the potential treatment of cerebral cavernous malformations; and
OV350, the first candidate from the Company’s library of KCC2
activators. His efforts will additionally characterize the medical
potential of a unique library of direct KCC2 transporter activators
in a range of indications, including epilepsies as well as other
cognitive, behavioral and pain disorders.
Prior to joining Ovid, Dr. Zhong served in
senior leadership and scientific roles at Generation Bio, Wave Life
Sciences, Vertex Pharmaceuticals, and GlaxoSmithKline
Pharmaceuticals. He has extensive neuroscience experience across
small molecule and next generation modalities and has been
responsible for developing scientific strategies and external
research collaborations. He earned a Ph.D. in Molecular Cell
Biology from The Rockefeller University in New York, where he
discovered Stat3 and Stat4. He completed his Postdoctoral Fellow in
the laboratory of Dr. Richard Axel at Columbia University.
Dr. Zhong will partner closely with Dr. Manoj
Malhotra who is taking on an expanded role as Chief Medical
Officer. Dr. Malhotra will oversee the Company’s clinical, medical,
and regulatory functions, and is responsible for progressing Ovid’s
clinical-stage programs. Drs. Malhotra and Zhong replace former
Head of Research & Development, Dr. Claude Nicaise, who is
retiring after seven years of service at Ovid. Dr. Nicaise will
continue to consult for the Company as a member of Ovid’s
Scientific Advisory Board (SAB).
“We are grateful to Claude for all he has done
for Ovid. It has been a privilege working alongside him daily and
we look forward to continuing to benefit from his wisdom and
experience in his continued collaboration via our SAB,” said Dr.
Levin. “Claude is among the select few in our industry who have
successfully stewarded medicines that have successfully saved and
extended lives. His thinking is embedded in our pipeline. We expect
to build on his leadership as we advance our programs,” said Dr.
Levin.
Corporate Strategy & Leadership
Appointment
In addition to deepening its bench of scientific
leadership, Ovid expanded the role of Meg Alexander to the position
of Chief Strategy Officer. In this remit, she will oversee Ovid’s
corporate strategy and planning, performance measurement, and risk
mitigation. She will also continue to oversee Ovid’s Corporate
Affairs function with a focus on effectively engaging the Company’s
stakeholders including the patient, caregiver, advocacy, and
policymaker communities that Ovid strives to serve. Prior to Ovid,
Ms. Alexander founded and led a consultancy group at Syneos Health,
one of the world’s largest clinical and commercial research
organizations, where she worked extensively with biopharmaceutical
C-suites and supported the launch efforts of approximately 25 rare
disease therapies.
General & Administrative
Infrastructure Cost Reductions & Operational
Efficiencies
In June 2023, Ovid made several changes and
reductions to its G&A functions to reduce infrastructure costs
and enhance efficiency as part of an ongoing operational
initiative. The Company continues to expect that its capital should
fund operations into the first half of 2025. Additionally, Ovid is
eligible for significant milestones and royalties if soticlestat is
approved and commercialized, which would serve as a long-term and
non-dilutive capital source for the Company. Ovid will continue to
operate efficiently and focus its capital and human resources
toward value-creating research and development efforts.
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 candidates seeks to meaningfully improve the lives of
people and families affected by rare epilepsies and seizure-related
disorders. Ovid intends to develop: a potential platform of potent
and highly selective ROCK2 inhibitors for the potential treatment
of rare neurological conditions, including GV101 for the potential
treatment of cerebral cavernous malformations; 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 StatementsThis
press release includes certain disclosures that contain
“forward-looking statements,” including, without limitation: the
creation of a leading R&D team and pipeline in the field of
seizures; the impact our appointments will have on our pipeline,
programs and our long-term success; statements regarding the
Company’s pipeline, including the potential development and use of
GV101, OV329, OV350, the library of ROCK2 inhibitors and the
library of KCC2 activator inhibitors; the status of Takeda’s two
pivotal Phase 3 trials evaluating soticlestat for Lennox-Gastaut
and Dravet syndromes; and the expectations and duration of Ovid’s
cash runway and the expectation that it will support the
advancement of Ovid’s pipeline. You can identify forward-looking
statements because they contain words such as "anticipates,"
"believes," "expected," "intends," "plan," "potentially," and
"will," and similar expressions (as well as other words or
expressions referencing future events, conditions or
circumstances). 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, the risk that Ovid may not be
able to realize the intended benefits of its technology. 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 Quarterly Report on Form 10-Q
filed with the Securities and Exchange Commission (SEC) on May 5,
2023, 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.
ContactsArgot PartnersMaeve
Conneighton212-596-7231ovid@argotpartners.com
Ovid Therapeutics (NASDAQ:OVID)
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