Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L01FX15

Blenrep(belantamab mafodotin)

Multiple Myeloma

Marketing Authorisation Holder: GlaxoSmithKline Trading Services Limited

EMA Authorisation: 23/07/2025

INN: belantamab mafodotin

Indication

Blenrep is indicated in adults for the treatment of relapsed or refractory multiple myeloma: in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy; and in combination with pomalidomide and dexamethasone in patients who have received at least one prior therapy including lenalidomide.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.