Drug intelligence / Profile preview

anlotinib + anti-PD-1 antibody

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

Overview

A combination therapy consisting of anlotinib, a novel oral multi-target tyrosine kinase inhibitor, and anti-PD-1 antibodies. Anlotinib inhibits vascular endothelial growth factor receptor (VEGFR) types 2 and 3, fibroblast growth factor receptor (FGFR) 1-4, platelet-derived growth factor receptor (PDGFR) α and β, stem cell factor receptor (c-Kit), and RET[1]. This combination creates synergistic effects by simultaneously targeting tumor angiogenesis and enhancing anti-tumor immunity. Research indicates that anlotinib can downregulate PD-L1 expression in cancer cells, which may enhance the effectiveness of anti-PD-1 therapy[4]. Additionally, anlotinib induces immunogenic cell death (ICD), elicits anti-tumor inflammation, and promotes infiltration and activation of dendritic cells and CD8+ T cells, effects that are further enhanced by anti-PD-1 antibodies[5].

02

Targets

AURKB (Aurora kinase B)VEGFR2 (Vascular endothelial growth factor receptor 2)PDCD1 (Programmed cell death protein 1 receptor)CSF1R (Macrophage colony-stimulating factor receptor)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR (FGFR family)RET (Rearranged during transfection receptor tyrosine kinase)DDR1 (Discoidin domain receptor 1)

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