Ovid Therapeutics Inc. announced results from its Phase 1 study of OV350, the first KCC2 direct activator dosed in humans. The study met its primary objectives, demonstrating safety, tolerability, and pharmacokinetics of OV350. The results from this study will be submitted for presentation at a future congress. Ovid also reported that it will not advance OV350 IV further in the clinic, instead prioritizing the development of its oral KCC2 direct activator programs, including OV4071 and OV4041. The company plans to submit a regulatory application for a Phase 1/1b clinical trial of OV4071 in the first quarter of 2026, with initiation of clinical studies expected in the second quarter of 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Ovid Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9604278-en) on December 18, 2025, and is solely responsible for the information contained therein.
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