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anlotinib + toripalimab + nab-paclitaxel
- Development stage
- Phase 2
- Lead developer
- Chia Tai-Tianqing Pharmaceutical Group
- Modality
- Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules, Nanoparticles → Drug Delivery Systems
- Administration
- Oral, Intravenous
01
Overview
This is a combination regimen consisting of three agents: anlotinib, toripalimab, and nab-paclitaxel. Anlotinib is a small molecule multi-targeted tyrosine kinase inhibitor that inhibits angiogenesis and tumor growth by targeting receptors such as VEGFR, PDGFR, FGFR, and c-KIT. Toripalimab is a monoclonal antibody immune checkpoint inhibitor targeting the programmed cell death protein 1 (PD-1) receptor to enhance anti-tumor immune responses. Nab-paclitaxel (nanoparticle albumin-bound paclitaxel) is a cytotoxic chemotherapeutic agent that stabilizes microtubules and inhibits cell division; its albumin-bound formulation improves drug delivery to tumors. The combination aims to synergistically inhibit tumor growth through antiangiogenic effects (anlotinib), immune activation (toripalimab), and direct cytotoxicity (nab-paclitaxel). This regimen has been investigated in phase II clinical trials for advanced or metastatic pancreatic cancer[1][6], with related studies in gastric cancer[2][4] and hepatocellular carcinoma[3].
- Brand names
- FukanghuaTuoyi
- Other names
- Anlotinib Plus Toripalimab and Nab-paclitaxel
02
Targets
FGFR1 (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)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)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)FGFR (FGFR family)TUBB (Tubulin (alpha and beta subunits))
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