Belantamab mafodotin (CAS RN 2050232-20-5) is a B-cell maturation antigen (BCMA)-directed antibody and microtubule inhibitor conjugate. Belantamab mafodotin is an antibody conjugate composed of 3 components 1) afucosylated, humanized immunoglobulin (Ig)G1 monoclonal antibody covalently linked to 2) the microtubule inhibitor monomethyl auristatin phenylalanine (MMAF) via 3) a protease-resistant maleimidocaproyl linker. The antibody is produced in a mammalian cell line (Chinese hamster ovary) using recombinant deoxyribonucleic acid (DNA) technology, and the microtubule inhibitor and linker are produced by chemical synthesis. Approximately 4 molecules of mafodotin are attached to each antibody molecule. The molecular weight of belantamab mafodotin is approximately 152 kDa.
Affygility Solutions has an occupational exposure limit (OEL) and control band assignment for this active pharmaceutical ingredient (API). This monograph also contains the acceptable daily exposure (ADE) value.
OEL Fastrac monographs are a cost-effective and convenient way to meet the requirements for PDEs (ADEs) contained in the EMA Guideline on setting health based exposure limits for use in risk identification in the manufacture of different medicinal products in shared facilities (EMA/CHMP/CVMP/SWP/169430/2012), as well as PIC/S and ANVISA requirements, and to obtain the following information:
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