Drug intelligence / Profile preview

chiauranib + etoposide

Development stage
Unknown
Lead developer
Akeso
Modality
Small Molecules
Administration
Oral
01

Overview

**chiauranib + etoposide** is a combination therapy comprising **chiauranib**, a novel small-molecule multi-targeted kinase inhibitor, and **etoposide**, a cytotoxic chemotherapy agent. Chiauranib selectively inhibits multiple kinase pathways, including *Vascular Endothelial Growth Factor Receptor* (VEGFR), *Aurora kinase B*, and *Colony Stimulating Factor 1 Receptor* (CSF-1R), thereby blocking tumor angiogenesis, regulating immune microenvironment, and interrupting cell cycle progression. Etoposide inhibits *topoisomerase II*, causing DNA breaks and apoptosis in rapidly dividing cells. The combination has shown enhanced antitumor efficacy and manageable safety in clinical trials for platinum-resistant or refractory ovarian cancer, with a focus on patients who have undergone multiple prior treatments. Primary clinical endpoints include progression-free survival and overall response rate.[1][2]

02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)AURKB (Aurora kinase B)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR-1 (Vascular endothelial growth factor receptor 1)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)TOP2A (DNA topoisomerase II)CSF1R (Macrophage colony-stimulating factor receptor)

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