Ovid Therapeutics And Graviton Bioscience Announces Topline Data From Phase 1 Clinical Trial Studying OV888/GV101 Capsule For Cerebral Cavernous Malformations
- The Phase 1 study for OV888/GV101 capsule met its objective, demonstrating a favorable safety and tolerability profile with no serious adverse events
- Secondary endpoint results indicate that the target pharmacokinetic profile was achieved at the targeted clinical dose, supporting once daily dosing
- OV888/GV101 capsule was shown to be biologically active in participants and elicited dose-dependent pharmacodynamic effects within the planned therapeutic dose range
- A Phase 2 study for the treatment of cerebral cavernous malformations is expected to initiate in the second half of 2024