Ovid Therapeutics Inc

NASDAQ OVID

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Ovid Therapeutics Inc Operating Cash Flow for the year ending December 31, 2023: USD -45.78 M

Ovid Therapeutics Inc Operating Cash Flow is USD -45.78 M for the year ending December 31, 2023, a 17.10% change year over year. Operating Cash Flow is the net cash generated from a company's core operations, including revenue, expenses, and changes in working capital.
  • Ovid Therapeutics Inc Operating Cash Flow for the year ending December 31, 2022 was USD -55.23 M, a -146.56% change year over year.
  • Ovid Therapeutics Inc Operating Cash Flow for the year ending December 31, 2021 was USD 118.61 M, a 329.94% change year over year.
  • Ovid Therapeutics Inc Operating Cash Flow for the year ending December 31, 2020 was USD -51.58 M, a -0.97% change year over year.
  • Ovid Therapeutics Inc Operating Cash Flow for the year ending December 31, 2019 was USD -51.09 M, a -12.14% change year over year.
NASDAQ: OVID

Ovid Therapeutics Inc

CEO Dr. Jeremy Max Levin Ba Zoology, Dphil, Mb Bchir
IPO Date May 5, 2017
Location United States
Headquarters 1460 Broadway, New York, NY, United States, 10036
Employees 40
Sector Healthcare
Industry Biotechnology
Description

Ovid Therapeutics Inc., a biopharmaceutical company, engages in the development of impactful medicines for patients and families with epilepsies and seizure-related neurological disorders in the United States. The company is developing soticlestat, a novel cholesterol 24 hydroxylase inhibitor, which is in Phase 3 clinical trials for the potential treatment of patients with resistant epilepsies; OV329, a GABA aminotransferase inhibitor which is in Phase 1 clinical trials for the treatment of seizures associated with tuberous sclerosis complex and infantile spasms; and OV350, a small molecule direct activator of the KCC2 transporter, which is in Phase 1 clinical trials for treating epilepsies. It also develops OV815, that focuses on the mutations associated with KIF1A-associated neurological disorder (KAND); OV888 (GV101), a highly selective rock2 inhibitor which is in Phase 1 double-blind multiple-ascending dose trial; OV825, has advanced to potential candidate lead identification for the rare neurodevelopmental condition HNRNPH2 (Bain Syndrome); and OV882, a short hairpin RNA gene therapy for the treatment of Angelman syndrome. The company has license and collaboration agreements with Healx, AstraZeneca AB, H. Lundbeck A/S, Northwestern University, and Graviton, as well as Marinus Pharmaceuticals, Inc. The company was incorporated in 2014 and is headquartered in New York, New York.

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September 20, 2024

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