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Seaport Therapeutics says Phase 1 trial shows GlyphAllo 375 mg does not impair next-morning driving vs placebo
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Seaport Therapeutics says Phase 1 trial shows GlyphAllo 375 mg does not impair next-morning driving vs placebo
  • Seaport Therapeutics reported positive topline Phase 1 driving simulator results for GlyphAllo, its oral prodrug of allopregnanolone.
  • Evening dosing at 375 mg showed no next-morning driving impairment versus placebo following multiple-day dosing; a single 250 mg dose also showed no impairment.
  • Zopiclone, used as a positive control, caused next-morning impairment, supporting the study’s ability to detect driving effects.
  • No serious adverse events were reported; most side effects were mild and transient.
  • Results will be submitted to the FDA; additional analyses are planned for future scientific meetings; BUOY-1 Phase 2b MDD topline data is expected in H1 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. Seaport Therapeutics Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 202609090700BIZWIRE_USPR_____20260909_BW055068) on September 09, 2026, and is solely responsible for the information contained therein.

Disclaimer:This article represents the opinion of the author only. It does not represent the opinion of Webull, nor should it be viewed as an indication that Webull either agrees with or confirms the truthfulness or accuracy of the information. It should not be considered as investment advice from Webull or anyone else, nor should it be used as the basis of any investment decision.
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