Drug intelligence / Profile preview

belantamab mafodotin + isatuximab

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

This is an **investigational combination therapy** comprising **belantamab mafodotin**, a B-cell maturation antigen (BCMA)-directed antibody-drug conjugate (ADC), and **isatuximab**, a CD38-directed monoclonal antibody. Belantamab mafodotin targets BCMA on malignant plasma cells, delivering the cytotoxic agent monomethyl auristatin-F (MMAF), which disrupts microtubules and induces apoptosis, while also engaging immune effectors via its afucosylated Fc region to stimulate antibody-dependent cellular cytotoxicity (ADCC) and phagocytosis. Isatuximab binds CD38 on multiple myeloma cells, promoting direct apoptosis, ADCC, complement-dependent cytotoxicity (CDC), and antibody-dependent cellular phagocytosis (ADCP). The combination is under clinical investigation for relapsed or refractory multiple myeloma based on preclinical and early clinical synergy, aiming to enhance anti-myeloma efficacy by dual targeting of the myeloma cell surface antigens and engaging multiple immune effector pathways[1][2][3][4][5][6][9].

Brand names
Blenrep (for belantamab mafodotin)Sarclisa (for isatuximab)
Other names
belantamab mafodotin plus isatuximabBlenrep plus Sarclisa
02

Targets

TUBB (Tubulin (alpha and beta subunits))CD38 (Cluster of Differentiation 38)BCMA (B-cell maturation antigen)

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