Drug intelligence / Profile preview

FOLFOX + cediranib

Development stage
Discontinued
Lead developer
AstraZeneca
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

FOLFOX + cediranib is a combination regimen consisting of the chemotherapy protocol FOLFOX (folinic acid [leucovorin], fluorouracil [5-FU], and oxaliplatin) plus the small molecule tyrosine kinase inhibitor cediranib. - **FOLFOX** is a standard chemotherapy regimen for colorectal cancer and other solid tumors. It works by combining agents that disrupt DNA synthesis (fluorouracil), enhance cytotoxicity (folinic acid), and cause DNA crosslinking leading to apoptosis (oxaliplatin). - **Cediranib** is an oral inhibitor of vascular endothelial growth factor receptor (VEGFR) tyrosine kinases, blocking angiogenesis required for tumor growth. Cediranib also inhibits platelet-derived growth factor receptors and c-Kit. The addition of cediranib to FOLFOX aims to combine direct cytotoxic effects with antiangiogenic therapy for enhanced antitumor activity[3][6][10].

Brand names
RECENTIN
Other names
FOLFOXfolinic acid + fluorouracil + oxaliplatin + cediranibleucovorin calcium + 5-fluorouracil + oxaliplatin + cediranib
02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)TS (Thymidylate synthase)VEGFR3 (Vascular endothelial growth factor receptor 3)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR-1 (Vascular endothelial growth factor receptor 1)DNAVEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRA (Platelet-derived growth factor receptor alpha)

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