Drug intelligence / Profile preview

dacetuzumab + rituximab + gemcitabine

Development stage
Discontinued
Lead developer
Skagen
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous
01

Overview

Dacetuzumab + rituximab + gemcitabine is a combination regimen studied for the treatment of relapsed or refractory diffuse large B-cell lymphoma (DLBCL)[1][5][7]. Dacetuzumab is a humanized monoclonal antibody targeting CD40, mediating its antitumor effect via effector cell functions (including antibody-dependent cellular cytotoxicity and phagocytosis) and direct apoptotic signal transduction[1][7]. Rituximab is a monoclonal antibody targeting CD20 on B-cells, leading to cell death primarily via immune-mediated mechanisms. Gemcitabine is a nucleoside antimetabolite chemotherapy that inhibits DNA synthesis in rapidly dividing cells[3][9]. The combination has shown synergistic activity in preclinical studies and promising response rates in phase 1b clinical trials for heavily pre-treated DLBCL patients[1][5][7]. Dacetuzumab is investigational and not approved for this indication. Common adverse events include nausea, thrombocytopenia, fatigue, headache, and cytokine release syndrome[1][7].

Brand names
Rituxan (rituximab)Gemzar (gemcitabine)
Other names
dacetuzumab + rituximab + gemcitabine
02

Targets

RNR (Ribonucleotide reductase)CD40 (Cluster of differentiation 40 receptor)CD20 (B-lymphocyte antigen CD20)

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