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EMA approval · 2025-11-24

EMA Authorised: Brukinsa (zanubrutinib) — BeOne Medicines Ireland Limited

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Summary

The European Medicines Agency authorised Brukinsa (zanubrutinib) for Waldenström macroglobulinemia, with BeOne Medicines Ireland Limited as the marketing author…

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Diseases / indications

Drugs mentioned

  • BRUKINSA (ZANUBRUTINIB)

Snippet

Status: Authorised. Therapeutic area: Waldenstrom Macroglobulinemia. MAH: BeOne Medicines Ireland Limited. Decision date: 24/10/2025