Drug intelligence / Profile preview

adebrelimab + anlotinib

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

Overview

Adebrelimab + anlotinib is a combination therapy comprising a programmed cell death ligand 1 (PD-L1) inhibitor and a multi-target tyrosine kinase inhibitor (TKI). Adebrelimab (SHR-1316), developed by Jiangsu Hengrui Pharmaceuticals, is a humanized IgG4 monoclonal antibody that blocks the interaction between PD-L1 and its receptors (PD-1 and B7.1), thereby enhancing T-cell mediated immune responses against tumor cells. Anlotinib (AL3818), developed by Chia Tai Tianqing, is an oral small molecule that inhibits multiple receptor tyrosine kinases involved in angiogenesis and tumor proliferation, including VEGFR1-3, FGFR1-4, PDGFRα/β, and c-Kit. This combination is primarily being investigated for the treatment of non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC), with clinical research often led by institutions such as Shanghai Pulmonary Hospital. The rationale for the combination lies in the potential synergistic effects of anti-angiogenic therapy in modulating the tumor microenvironment to enhance the efficacy of immune checkpoint inhibitors.

Brand names
AdelyFukanghua
Other names
SHR-1316 + AL3818
02

Targets

FGFR4 (Fibroblast growth factor receptor 4)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR3 (Fibroblast growth factor receptor 3)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR-1 (Vascular endothelial growth factor receptor 1)CD274 (Programmed cell death protein 1 ligand 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR1 (Fibroblast growth factor receptor 1)

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