Drug intelligence / Profile preview

bevacizumab + sunitinib

Development stage
Discontinued
Lead developer
Memorial Sloan Kettering Cancer Center
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

This combination therapy regimen consists of bevacizumab, a humanized monoclonal antibody targeting vascular endothelial growth factor (VEGF), and sunitinib, a multi-targeted small molecule tyrosine kinase inhibitor. Investigated primarily by Memorial Sloan Kettering Cancer Center (MSKCC) for the treatment of metastatic renal cell carcinoma (mRCC), the rationale was to provide continuous antiangiogenic blockade by using bevacizumab to prevent rebound angiogenesis during the standard two-week rest period of sunitinib. However, clinical trials (Phase I/II) revealed significant overlapping toxicities, including severe hypertension, hematologic issues, and vascular complications, leading to the discontinuation of further development of this specific combination at the tested dose levels.

Other names
Bevacizumab and SunitinibSunitinib and Bevacizumab
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRB (Platelet-derived growth factor receptor beta)CSF1R (Macrophage colony-stimulating factor receptor)VEGFA (Vascular endothelial growth factor A)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)PDGFRA (Platelet-derived growth factor receptor alpha)RET (Rearranged during transfection receptor tyrosine kinase)FLT3 (Fms related receptor tyrosine kinase 3)

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