EMA
approval
· 2026-01-14
EMA Authorised: Rydapt (Midostaurin) — Novartis Europharm Ltd
Summary
The European Medicines Agency authorised Rydapt (midostaurin) for additional indications in acute myeloid leukemia and systemic mastocytosis. The decision inclu…
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Leukemia, Myeloid, Acute;Mastocytosis. MAH: Novartis Europharm Ltd. Decision date: 13/01/2026. Orphan medicine