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EMA approval · 2026-07-10

EMA Authorised: Neofordex (dexamethasone) — THERAVIA

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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

  • Neofordex (dexamethasone)

Snippet

Status: Authorised. Therapeutic area: Multiple Myeloma. MAH: THERAVIA. Decision date: 09/07/2026