Daratumumab is an immunoglobulin (Ig) G1 kappa (G1κ) human monoclonal antibody (mAb) that binds to the cluster of differentiation (CD)38 antigen. It is produced in Chinese hamster ovary (CHO) cells using recombinant deoxyribonucleic acid (DNA) technology. The molecular weight of daratumumab is approximately 148 kDa. Daratumumab is a CD38-directed cytolytic antibody indicated intravenously (IV), alone or in combination with other medications, for the treatment of adult patients with multiple myeloma (MM). Subcutaneous (SC) daratumumab with hyaluronidase is also indicated, alone or in combination with other medications, for the treatment of MM, plasma-cell myeloma, and for the treatment of light chain (AL) amyloidosis.
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:
To order an OEL/ADE monograph for Daratumumab, just click the ADD TO CART button.
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Not the compound you were looking for? You can search the OEL Fastrac catalog to find more available compounds.
Affygility Solutions’ OEL Fastrac service is an user-friendly system that enables us to make confident decisions and focus on moving the compound safely through our facility. We can quickly access the database to determine if a new drug is within the OEL Fastrac library, and if so, immediately download a detailed OEL banding report. The OEL Fastrac system has been a helpful tool in our overall EH&S program.