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Denintuzumab mafodotin is a humanized monoclonal antibody-drug conjugate (ADC) developed for the treatment of CD19-positive B-cell malignancies, including acute lymphoblastic leukemia (ALL) and non-Hodgkin lymphoma. The drug consists of an anti-CD19 monoclonal antibody linked to the cytotoxic agent monomethyl auristatin F (MMAF). Upon binding to CD19 on B cells, the ADC is internalized, releasing MMAF inside the cell. MMAF binds to tubulin and inhibits its polymerization, resulting in G2/M phase cell cycle arrest and apoptosis of tumor cells. Denintuzumab mafodotin was developed by Seattle Genetics and has been evaluated in clinical trials for relapsed or refractory B-cell non-Hodgkin lymphoma and ALL[1][4][6].
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