Ovid Therapeutics Inc

NASDAQ OVID

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Ovid Therapeutics Inc Free Cash Flow Per Share for the Trailing 12 Months (TTM) ending March 31, 2024: -0.24

Ovid Therapeutics Inc Free Cash Flow Per Share is -0.24 for the Trailing 12 Months (TTM) ending March 31, 2024, a -36.93% change year over year. Free Cash Flow per Share represents the amount of free cash flow generated per outstanding share of common stock. It provides insight into the per-share value of free cash flow and is commonly used in valuation analysis. A higher value suggests a potentially more favorable investment opportunity.
  • Ovid Therapeutics Inc Free Cash Flow Per Share for the Trailing 12 Months (TTM) ending March 31, 2023 was -0.17, a 24.30% change year over year.
  • Ovid Therapeutics Inc Free Cash Flow Per Share for the Trailing 12 Months (TTM) ending March 31, 2022 was -0.23, a -149.20% change year over year.
  • Ovid Therapeutics Inc Free Cash Flow Per Share for the Trailing 12 Months (TTM) ending March 31, 2021 was 0.46, a 249.25% change year over year.
  • Ovid Therapeutics Inc Free Cash Flow Per Share for the Trailing 12 Months (TTM) ending March 31, 2020 was -0.31, a 29.52% 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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StockViz Staff

September 20, 2024

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