Cognition Therapeutics Schedules a Type C Meeting with FDA to Align on Endpoints for Phase 3 Trial of Zervimesine (CT1812) in DLB
Cognition Therapeutics has scheduled a Type C meeting with the FDA's Division of Neurology for October 20th to align on endpoints for the Phase 3 trial of Zervimesine (CT1812) in dementia with Lewy bodies (DLB). The meeting is expected to define the endpoint for the Phase 3 study.
Why it matters — A CGTX watcher would care because the FDA meeting outcome will shape the design and endpoint of the company's Phase 3 trial for Zervimesine in DLB, a key step in its clinical development.