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EMA approval · 2026-02-19

EMA Authorised: Adzynma (rADAMTS13) — Takeda Manufacturing Austria AG

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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

  • Adzynma

Snippet

Status: Authorised. Therapeutic area: Purpura, Thrombotic Thrombocytopenic. MAH: Takeda Manufacturing Austria AG. Decision date: 09/01/2026. Orphan medicine