Drug intelligence / Profile preview

sintilimab + anlotinib + chemotherapy

Development stage
Phase 3
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

**Sintilimab + anlotinib + chemotherapy** is an investigational combination cancer regimen that pairs the PD-1 immune checkpoint inhibitor sintilimab with the oral multitarget tyrosine kinase inhibitor anlotinib and a cytotoxic chemotherapy backbone. Sintilimab is a fully human IgG4 monoclonal antibody that blocks the interaction between PD-1 and its ligands (PD-L1 and PD-L2), thereby restoring T-cell-mediated antitumor immunity. Anlotinib is a small-molecule inhibitor targeting multiple receptor tyrosine kinases, including VEGFR1/2/3, FGFR1-4, PDGFR-alpha/beta, and c-Kit, which suppresses tumor angiogenesis and cell proliferation. The chemotherapy backbone varies depending on the clinical study and tumor type (e.g., nab-paclitaxel, gemcitabine/cisplatin, or albumin paclitaxel plus nedaplatin) to directly induce tumor cell death. This triplet regimen is being evaluated in Phase 2 clinical trials for various solid tumors, including non-small cell lung cancer (NSCLC), extensive-stage small cell lung cancer (ES-SCLC), biliary tract cancer (BTC), esophageal cancer, and triple-negative breast cancer (TNBC), demonstrating promising synergistic efficacy and manageable safety profiles.

Other names
sintilimab plus anlotinib plus chemotherapysintilimab, anlotinib, and chemotherapysintilimab/anlotinib/chemotherapy
02

Targets

DNAFGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)PDCD1 (Programmed cell death protein 1 receptor)CD274 (Programmed cell death protein 1 ligand 1)PDCD1LG2 (Programmed cell death 1 ligand 2)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)TUBB (Tubulin (alpha and beta subunits))

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