FDA Grants Fast Track Designation to MapLight Therapeutics' ML-007C-MA for Alzheimer's Psychosis

Reuters

Jan 05

FDA Grants <a href="https://laohu8.com/S/FTRK">Fast Track</a> Designation to MapLight <a href="https://laohu8.com/S/LENZ">Therapeutics</a>' ML-007C-MA for Alzheimer's Psychosis

MapLight Therapeutics Inc. announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to its investigational drug ML-007C-MA for the treatment of hallucinations and delusions associated with Alzheimer's disease psychosis $(ADP)$. The Fast Track designation is intended to facilitate the development and expedite the review of therapies for serious conditions with unmet medical needs. ML-007C-MA is currently being evaluated in the ongoing Phase 2 VISTA clinical trial, with topline results expected in the second half of 2027.

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. Maplight Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9619531-en) on January 05, 2026, and is solely responsible for the information contained therein.

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The Fast Track designation is intended to facilitate the development and expedite the review of therapies for serious conditions with unmet medical needs. ML-007C-MA is currently being evaluated in the ongoing Phase 2 VISTA clinical trial, with topline results expected in the second half of 2027.\n      \n\n\nDisclaimer: 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. Maplight Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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