Blenrep® (belantamab mafodotin-blmf)

BL 761158

Blenrep® (belantamab mafodotin-blmf)

BL 761158

U.S. License Holder:

GlaxoSmithKline

Date of License:

August-05-2020

Last Update:

Nov-15-2024

approved_indications FDA-Approved Indications

BLENREP (belantamab mafodotin-blmf) is a B-cell maturation antigen (BCMA)-directed antibody and microtubule inhibitor conjugate indicated for the treatment of adult patients with relapsed or refractory multiple myeloma who have received at least 4 prior therapies including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulatory agent.

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Methodology

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