EMA
approval
· 2025-12-19
EMA Authorised: Replagal (agalsidase alfa) — Takeda Pharmaceuticals International AG Ireland Branch
Summary
The EMA authorised Replagal (agalsidase alfa) for treatment of Fabry disease, with Takeda Pharmaceuticals International AG Ireland Branch as the marketing autho…
Upgrade for the full analysis, importance score, and drug timeline.
Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Fabry Disease. MAH: Takeda Pharmaceuticals International AG Ireland Branch. Decision date: 17/12/2025