FDA approves belantamab mafodotin-blmf for relapsed or refractory multiple myeloma

FDA

23 October 2025 - Today, the FDA approved belantamab mafodotin-blmf (Blenrep, GlaxoSmithKline), a B-cell maturation antigen (BCMA)-directed antibody and microtubule inhibitor conjugate, with bortezomib and dexamethasone for adults with relapsed or refractory multiple myeloma who have received at least two prior lines of therapy, including a proteasome inhibitor and an immunomodulatory agent.

Efficacy was evaluated in DREAMM-7, an open-label, randomised, multi-centre trial in adults with relapsed or refractory multiple myeloma who had received at least one line of prior therapy.

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Michael Wonder

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Michael Wonder

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Cancer , Outcome , Medicine , US , Registration