Ovid Therapeutics reported a revenue of $148,000 and a net loss of $11.7 million for the first quarter ended March 31, 2024. The company's cash, cash equivalents, and marketable securities totaled $90.3 million as of March 31, 2024, which is expected to support operations into H1 2026. Takeda has completed two Phase 3 trials studying soticlestat.
Takeda completed two Phase 3 trials for soticlestat, with topline data expected in Takeda's H1 2024 fiscal year.
Phase 1 trial for OV888 (GV101) is complete, with topline safety data expected in H1 2024.
Ovid expects to initiate a Phase 2 clinical program for OV888 (GV101) in cerebral cavernous malformations in H2 2024.
Cash, cash equivalents, and marketable securities were $90.3 million as of March 31, 2024, supporting operations into H1 2026.
Ovid anticipates its cash runway will support operations and clinical development programs into H1 2026. During this time, Ovid anticipates several events for its current pipeline programs as well as clinical and regulatory results for soticlestat from Takeda.