Drug intelligence / Profile preview

bevacizumab + sorafenib

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

Overview

Bevacizumab + sorafenib is an investigational combination therapy consisting of two distinct anticancer agents with complementary mechanisms of action. Bevacizumab is a humanized monoclonal antibody that targets and neutralizes vascular endothelial growth factor A (VEGF-A), thereby inhibiting angiogenesis—the formation of new blood vessels essential for tumor growth. Sorafenib is a small molecule multikinase inhibitor that blocks several intracellular and cell surface kinases involved in tumor cell proliferation and angiogenesis, including RAF kinases, VEGF receptors (VEGFR-1/2/3), platelet-derived growth factor receptor beta (PDGFR-β), FLT3, c-KIT, and RET. The rationale for combining these agents is to achieve more comprehensive inhibition of angiogenic pathways in cancer treatment. This combination has been studied primarily in advanced hepatocellular carcinoma (HCC) as well as other solid tumors such as ovarian cancer[1][8]. However, clinical trials have reported increased toxicity without clear evidence of superior efficacy compared to standard therapies.

Brand names
Nexavar
Other names
bevacizumab and sorafenibsorafenib plus bevacizumab
02

Targets

RAF1 (c-Raf-1 (Y340D/Y341D))KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)VEGFA (Vascular endothelial growth factor A)VEGFR2 (Vascular endothelial growth factor receptor 2)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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