Drug intelligence / Profile preview

sunitinib + paclitaxel

Development stage
Phase 3
Lead developer
Pfizer
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Sunitinib + paclitaxel is a combination of two pharmaceutical agents used in oncology clinical trials. Sunitinib is an oral small-molecule multi-targeted receptor tyrosine kinase (RTK) inhibitor that blocks several RTKs involved in tumor growth, angiogenesis, and metastatic progression, including platelet-derived growth factor receptors (PDGFRs), vascular endothelial growth factor receptors (VEGFRs), KIT, FLT3, RET, and CSF-1R. Paclitaxel is a cytotoxic chemotherapeutic agent that stabilizes microtubules and inhibits cell division. The combination has been investigated for the treatment of advanced solid tumors such as metastatic breast cancer and angiosarcoma. Preclinical studies suggest enhanced anti-tumor activity through both antiangiogenic effects from sunitinib and cytotoxicity from paclitaxel[1][2][3].

02

Targets

CSF1R (Macrophage colony-stimulating factor receptor)FLT3 (Fms related receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)PDGFRB (Platelet-derived growth factor receptor beta)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)GFRA4 (GDNF family receptor alpha-4)TUBB (Tubulin (alpha and beta subunits))

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