Drug intelligence / Profile preview

crizotinib + sorafenib

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral
01

Overview

Crizotinib + sorafenib is a combination of two small molecule kinase inhibitors used primarily in oncology research. Crizotinib is a tyrosine kinase inhibitor targeting anaplastic lymphoma kinase (ALK), ROS1, hepatocyte growth factor receptor (c-MET), and Recepteur d’Origine Nantais (RON). It is approved for the treatment of ALK-positive or ROS1-positive non-small cell lung cancer, as well as ALK-positive anaplastic large cell lymphoma and inflammatory myofibroblastic tumor[5][6]. Sorafenib is a multikinase inhibitor that targets cell surface tyrosine kinase receptors and downstream kinases involved in tumor proliferation and angiogenesis, including RAF kinases, VEGFR, PDGFR, c-KIT, FLT-3, and RET. It is approved for unresectable hepatocellular carcinoma, advanced renal cell carcinoma, and differentiated thyroid carcinoma[4][8]. The combination has been studied preclinically for synergistic antitumor effects; co-delivery in animal models showed reduced tumor development and improved survival compared to single agents[2][3].

Brand names
Nexavar
Other names
crizotinib + sorafenib
02

Targets

ALK (Anaplastic lymphoma kinase receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)AXL (AXL receptor tyrosine kinase)ER-XBRAF (B-Raf proto-oncogene, serine/threonine kinase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)MET (Mesenchymal-epithelial transition factor receptor)ROS1 (Proto-oncogene tyrosine-protein kinase ROS)EPH (EPH receptor family)RAF1 (c-Raf-1 (Y340D/Y341D))PDGFRB (Platelet-derived growth factor receptor beta)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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