Drug intelligence / Profile preview

urelumab + nivolumab

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Urelumab + nivolumab is an investigational combination therapy consisting of two monoclonal antibodies used in cancer immunotherapy. Urelumab is a fully human IgG4 monoclonal antibody that acts as an agonist of CD137 (also known as 4-1BB), a co-stimulatory receptor on activated T cells and natural killer (NK) cells. By activating CD137 signaling, urelumab enhances the proliferation and cytotoxic activity of immune effector cells against tumor cells. Nivolumab is a fully human IgG4 monoclonal antibody that blocks the programmed death-1 (PD-1) receptor on T cells, thereby preventing inhibitory signaling and promoting T cell-mediated antitumor responses. The combination aims to synergistically enhance antitumor immunity by simultaneously stimulating immune activation through CD137 and relieving immune suppression via PD-1 blockade. This regimen has been studied in early-phase clinical trials for various advanced solid tumors and hematologic malignancies including melanoma, non-small cell lung cancer (NSCLC), head and neck squamous cell carcinoma, B-cell lymphoma, bladder cancer, and pancreatic adenocarcinoma[3][4][5][7].

Brand names
Opdivo
Other names
anti-CD137 antibody + anti–PD-1 antibodyurelumab plus nivolumab
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)TNFRSF9 (CD137 extracellular domain)

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