Drug intelligence / Profile preview

belantamab mafodotin + elotuzumab

Development stage
Unknown
Lead developer
GSK
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Belantamab mafodotin + elotuzumab is an investigational combination therapy being evaluated for the treatment of relapsed or refractory multiple myeloma. Belantamab mafodotin is a B-cell maturation antigen (BCMA)-targeted antibody-drug conjugate (ADC) that delivers the cytotoxic agent monomethyl auristatin F (MMAF) directly to plasma cells, inducing apoptosis and enhancing immune-mediated cell death. Elotuzumab is a humanized monoclonal antibody targeting Signaling Lymphocytic Activation Molecule Family member 7 (SLAMF7), which activates Natural Killer (NK) cells and tags myeloma cells for antibody-dependent cellular cytotoxicity (ADCC). This combination, currently being studied in the Phase Ib/II Bela-Elo trial sponsored by Yale University in collaboration with GSK, aims to leverage synergistic immune-mediated mechanisms to overcome resistance in heavily pretreated, triple-class refractory patients.

Brand names
BlenrepEmpliciti
Other names
belantamab mafodotin-blmfBela-Elo
02

Targets

SLAMF7 (Signaling lymphocytic activation molecule family member 7)BCMA (B-cell maturation antigen)

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