EMA
approval
· 2026-07-10
EMA Authorised: Neofordex (dexamethasone) — THERAVIA
Summary
European Medicines Agency authorised Neofordex (dexamethasone) for therapeutic use, with THERAVIA as the marketing authorization holder, in multiple myeloma.
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Diseases / indications
Drugs mentioned
Snippet
Status: Authorised. Therapeutic area: Multiple Myeloma. MAH: THERAVIA. Decision date: 09/07/2026