- Amylyx reported completion of enrollment in the Phase 3 LUCIDITY trial evaluating avexitide for post-bariatric hypoglycemia after Roux-en-Y gastric bypass surgery.
- The randomized, double-blind, placebo-controlled study is 16 weeks long and enrolled 78 participants.
- The primary endpoint is reduction in the composite of Level 2 and Level 3 hypoglycemic events through Week 16.
- Topline results have not yet been presented and are expected in Q3 2026.
- Participants who complete the double-blind period may enter a 32-week open-label extension.
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. Amylyx Pharmaceuticals Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20260324658631) on March 24, 2026, and is solely responsible for the information contained therein.
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