Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Lenvatinib + sintilimab is a combination therapy consisting of two agents: lenvatinib, an oral small molecule multikinase inhibitor, and sintilimab, a monoclonal antibody targeting the programmed cell death protein 1 (PD-1). Lenvatinib inhibits multiple receptor tyrosine kinases involved in tumor angiogenesis and proliferation, including vascular endothelial growth factor receptors (VEGFR1–3), fibroblast growth factor receptors (FGFR1–4), platelet-derived growth factor receptor alpha (PDGFRα), RET, and KIT. Sintilimab blocks PD-1 on T cells to enhance antitumor immune responses by preventing its interaction with PD-L1/PD-L2. The combination leverages both antiangiogenic effects and immune checkpoint inhibition for synergistic antitumor activity. This regimen has been investigated primarily in advanced hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (iCCA) as second-line or conversion therapy after chemotherapy failure or for patients unsuitable for surgery[1][2][10].
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 lenvatinib + sintilimab.