Cognition Therapeutics plans late-stage zervimesine trial for Lewy body dementia psychosis
Cognition Therapeutics, Inc.
Cognition Therapeutics, Inc. CGTX | 0.00 |
- Cognition Therapeutics met the FDA on May 20, 2026 to review Phase 2 results for zervimesine (CT1812) in dementia with Lewy bodies patients with psychosis, outlining a proposed registrational study.
- The discussion was described as positive, supporting a path forward to move the drug into a late-stage program for this indication.
- Formal FDA meeting minutes are expected in June, setting up the next decision point for the registrational trial design and endpoints.
- The company also noted zervimesine is being studied in the Phase 2 START trial in mild cognitive impairment and early Alzheimer’s disease.
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. Cognition Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202605210730PRIMZONEFULLFEED9724360) on May 21, 2026, and is solely responsible for the information contained therein.
