Amylyx to present Phase 1 AMX0114 data at ENCALS 2026
The LUMINA trial showed no drug-related serious adverse events in Cohort 1, supporting further study.
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Biopharmaceutical company developing novel therapies
amylyx.comLast updated
In short: Amylyx Pharmaceuticals advanced its rare disease pipeline and resolved major litigation while transitioning its lead programs in 2025-2026.
The LUMINA trial showed no drug-related serious adverse events in Cohort 1, supporting further study.
Week 24 and 48 results show improved pancreatic function and visual acuity stabilization, with favorable safety.
R&D expenses rise to $27.6M, net loss $41.3M. LUCIDITY trial enrollment complete, topline data expected Q3 2026. Cash runway into 2028.
The program provides access to eligible adults with post-bariatric hypoglycemia following Roux-en-Y gastric bypass. Avexitide is in Phase 3 LUCIDITY trial with data expected Q3 2026.
Amylyx will read out results for a rare endocrine disorder treatment, a pivotal moment.
Amylyx Pharmaceuticals, Inc. (Nasdaq: AMLX) (“Amylyx” or the “Company”) today announced the pricing of an underwritten public offering of 17,142,857 shares of its common stock...
Halper Sadeh LLC, an investor rights law firm, is investigating whether certain officers and directors of Amylyx Pharmaceuticals, Inc. (NASDAQ: AMLX) breached their fiduciary duties...
Here is STAT’s biotech scorecard, our regular ledger of stock-moving biotech events, for the third quarter.
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