EMA
approval
· 2026-01-23
EMA Authorised: Nexviadyme (avalglucosidase alfa) — Sanofi B.V.
Summary
EMA authorised Nexviadyme (avalglucosidase alfa) from Sanofi B.V. for Pompe disease (Glycogen Storage Disease Type II) with decision dated 06/08/2024.
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Glycogen Storage Disease Type II. MAH: Sanofi B.V.. Decision date: 06/08/2024