Drug intelligence / Profile preview

axitinib + FOLFOX

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

Overview

Axitinib + FOLFOX is a **combination regimen** consisting of axitinib, a potent and selective second-generation inhibitor of vascular endothelial growth factor receptors (VEGFR 1, 2, and 3), together with the FOLFOX chemotherapy regimen, which includes folinic acid (leucovorin), fluorouracil (5-FU), and oxaliplatin. The combination targets tumor angiogenesis and directly cytotoxic effects on cancer cells. Axitinib acts by blocking VEGF-mediated signaling to inhibit angiogenesis in tumors, while FOLFOX impairs DNA replication, repair, and cell division in rapidly dividing cancer cells. This regimen has been investigated primarily for the treatment of advanced gastrointestinal cancers, particularly metastatic colorectal cancer, in phase I and II trials. The combination has been shown to be generally well tolerated, with adverse events manageable and pharmacokinetic interactions absent[1][3][5].

Other names
axitinib plus FOLFOXaxitinib + FOLFOXaxitinib combined with FOLFOX
02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)DNAPDGFRB (Platelet-derived growth factor receptor beta)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)TS (Thymidylate synthase)

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