Prognia
Drug Database
🇪🇺EU · EMAExpiredATC: L01XC39Orphan MedicineConditional Approval

Blenrep(belantamab mafodotin)

Multiple Myeloma

Marketing Authorisation Holder: GlaxoSmithKline Trading Services Limited

EMA Authorisation: 25/08/2020

INN: belantamab mafodotin

Indication

Blenrep is indicated as monotherapy for the treatment of multiple myeloma in adult patients, who have received at least four prior therapies and whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and an anti-CD38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

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.