Acadia's remlifanserin narrowly misses primary endpoint in Phase 2 Alzheimer's psychosis study
The company will proceed to Phase 3 with the 60 mg dose and drop the 30 mg arm after mixed Phase 2 RADIANT results.
SEC filing
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The company will proceed to Phase 3 with the 60 mg dose and drop the 30 mg arm after mixed Phase 2 RADIANT results.
SEC filing
The company also detailed the separation terms for former CEO Daniel Vitt as he transitions to a consulting and advisory role.
SEC filing
The company also completed Phase 2 enrollment in its remlifanserin Alzheimer's psychosis program and won FDA Fast Track designation, with topline data expected in September to October 2026.
SEC filing