EMA
approval
· 2026-02-19
EMA Authorised: Adzynma (rADAMTS13) — Takeda Manufacturing Austria AG
Summary
The European Medicines Agency authorized Adzynma (rADAMTS13) for the treatment of thrombotic thrombocytopenic purpura and granted orphan medicine status.
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Purpura, Thrombotic Thrombocytopenic. MAH: Takeda Manufacturing Austria AG. Decision date: 09/01/2026. Orphan medicine