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Amylyx Pharmaceuticals, Inc.: Amylyx Pharmaceuticals Announces EMA Validation of Marketing Authorisation Application (MAA) for AMX0035 for the Treatment of ALS

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 ....

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Fixed-Dose Combo Therapy for Amyotrophic Lateral Sclerosis Gets Priority Review

The FDA has accepted for Priority Review the New Drug Application for AMX0035 (sodium phenylbutyrate and taurursodiol) for the treatment of ALS. ....

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Amylyx Pharmaceuticals Announces FDA Acceptance and Priority Review of New Drug Application (NDA) for AMX0035 for the Treatment of ALS

Press release content from Business Wire. The AP news staff was not involved in its creation. ....

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