Drug intelligence / Profile preview

pembrolizumab + anlotinib

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

Overview

A combination therapy consisting of the anti-PD-1 monoclonal antibody pembrolizumab and the multi-targeted tyrosine kinase inhibitor anlotinib. Pembrolizumab is an immune checkpoint inhibitor that blocks the interaction between PD-1 and its ligands (PD-L1 and PD-L2), thereby enhancing T-cell mediated anti-tumor immune responses. Anlotinib is a small molecule inhibitor that targets multiple receptor tyrosine kinases, including vascular endothelial growth factor receptors (VEGFR1-3), fibroblast growth factor receptors (FGFR1-4), platelet-derived growth factor receptors (PDGFRα/β), and c-Kit, primarily acting as an anti-angiogenic agent. This combination is being investigated by The Affiliated Hospital of Qingdao University for the treatment of recurrent or refractory high-grade serous ovarian cancer (HGSOC), aiming to leverage the synergistic effects of anti-angiogenesis and immune checkpoint blockade to overcome resistance in platinum-resistant or refractory patients. Early trial results presented at the 2022 ASCO Annual Meeting showed promising efficacy with a median progression-free survival of 13.0 months and an objective response rate of 33.3% in this patient population.

Brand names
Keytruda
Other names
pembrolizumab plus anlotinib
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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