Neurocrine Biosciences Inc. has announced the initiation of a Phase 2 clinical study evaluating its investigational compound NBI-1065890 in adults with tardive dyskinesia $(TD)$. NBI-1065890 is a next-generation, selective VMAT2 inhibitor designed to potentially offer a differentiated and longer-acting treatment option for TD. The randomized, double-blind, placebo-controlled study will enroll approximately 100 adult participants and will assess efficacy, safety, and tolerability over eight weeks, with the primary endpoint being the change in Abnormal Involuntary Movement Scale (AIMS) dyskinesia total score. The research is ongoing, and results have not yet been presented.
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. Neurocrine Biosciences Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: LA70235) on January 26, 2026, and is solely responsible for the information contained therein.
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