Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Nivolumab + pazopanib** is an investigational combination regimen of two pharmaceutical agents: nivolumab, a fully human IgG4 monoclonal antibody targeting the programmed death-1 (PD-1) immune checkpoint, and pazopanib, a small molecule multi-targeted tyrosine kinase inhibitor (TKI) with activity primarily against vascular endothelial growth factor receptors (VEGFR), platelet-derived growth factor receptors (PDGFR), and c-Kit. Nivolumab acts as an immune checkpoint inhibitor, reversing T-cell suppression in the tumor microenvironment by blocking the PD-1 pathway, thus enhancing antitumor immune responses. Pazopanib inhibits tumor angiogenesis and cell proliferation via blockade of VEGFR and related kinases. The combination has been evaluated in clinical trials for advanced or metastatic renal cell carcinoma (RCC) and relapsed/metastatic sarcoma. Early trials showed some antitumor activity, but the regimen was associated with a high incidence of grade 3/4 toxicities, particularly hepatotoxicity, resulting in early trial closure for this combination and limited further development[1][3][5][7].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on nivolumab + pazopanib.