Amylyx Pharmaceuticals, Inc. (Nasdaq: AMLX) ("Amylyx" or the "Company"), today announced that its Marketing Authorisation Application (MAA) to the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) for AMX0035 (sodium phenylbutyrate [PB] and ursodoxicoltaurine [TURSO; also known as taurursodiol]) for the treatment of amyotrophic lateral sclerosis (ALS) has been validated and is now under CHMP review.
https://finance.yahoo.com/news/amylyx-pharmaceuticals-announces-ema-validation-130000735.html
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