Drug intelligence / Profile preview

denintuzumab mafodotin

Development stage
Phase 1
Lead developer
Skagen
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

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].

Other names
denintuzumab mafodotinCys-McMMAF
02

Targets

CD19 (B lymphocyte antigen CD19)TUBB (Tubulin (alpha and beta subunits))

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