ACADIA Pharmaceuticals IncACAD
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FDA Fast Track designation accelerates development and review for remlifanserin in Alzheimer's psychosis.

The U.S. Food and Drug Administration has granted Fast Track designation to Acadia Pharmaceuticals' remlifanserin for the treatment of hallucinations and delusions associated with Alzheimer's disease psychosis. Acadia also announced that enrollment in the Phase 2 portion of its RADIANT program evaluating remlifanserin for ADP has been completed, with topline results expected between September and October 2026. Acadia shares rose nearly 2% in pre-market trading after closing at $25.60 on Friday.
ACADIA Pharmaceuticals IncFDA Fast Track designation accelerates development and review for remlifanserin in Alzheimer's psychosis.