Drug intelligence / Profile preview

tivantinib + sorafenib

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

Overview

**Tivantinib (ARQ 197) is a selective non-ATP competitive inhibitor of c-MET, a receptor tyrosine kinase implicated in tumor cell proliferation, invasion, and angiogenesis. Sorafenib is a multikinase inhibitor that targets several kinases involved in tumor cell signaling and angiogenesis, including Raf serine/threonine kinases (Raf-1/C-Raf and B-Raf), VEGFRs (vascular endothelial growth factor receptors), PDGFR-β (platelet-derived growth factor receptor beta), KIT, FLT3, and RET. The combination of tivantinib and sorafenib has been investigated for synergistic antitumor effects in various cancers such as hepatocellular carcinoma (HCC), renal cell carcinoma (RCC), melanoma, breast cancer, non-small cell lung cancer (NSCLC), and pancreatic adenocarcinoma. Tivantinib enhances the antitumor effect of sorafenib by decelerating its clearance in HCC cells through inhibition of PXR activation. This combination has shown manageable safety profiles in early-phase clinical trials with some dose-limiting toxicities observed at higher doses.**

Brand names
Nexavar
Other names
ARQ 197 + sorafenibtivantinib + sorafenib
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)MET (Mesenchymal-epithelial transition factor receptor)BRAF (B-Raf proto-oncogene, serine/threonine kinase)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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