Drug intelligence / Profile preview

cediranib + cisplatin + S-1

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

Overview

Combination therapy of **cediranib**, **cisplatin**, and **S-1** is an investigational anti-cancer regimen for advanced gastric cancer and potentially other solid tumors. Cediranib is a small molecule tyrosine kinase inhibitor targeting vascular endothelial growth factor receptors (VEGFRs), impeding tumor angiogenesis. Cisplatin is a platinum-based chemotherapeutic agent that forms DNA crosslinks, leading to apoptosis. S-1 is an oral fluoropyrimidine derivative comprised of tegafur, gimeracil, and oteracil, primarily inhibiting thymidylate synthase to disrupt DNA synthesis. This triple regimen is being evaluated for safety and efficacy, showing tolerability and preliminary anti-tumor activity in phase I trials for advanced gastric cancer[1][2][4].

02

Targets

DNAPDGFRB (Platelet-derived growth factor receptor beta)TS (Thymidylate synthase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFR (PDGFR family)

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