Drug intelligence / Profile preview

docetaxel + vandetanib

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

Overview

Docetaxel + vandetanib is a combination therapy that pairs docetaxel, a taxane chemotherapeutic agent, with vandetanib, a tyrosine kinase inhibitor. Vandetanib inhibits vascular endothelial growth factor receptor 2 (VEGFR-2), epidermal growth factor receptor (EGFR), and RET tyrosine kinases. The combination alters the balance of proapoptotic and prosurvival proteins, potentially enhancing docetaxel-induced apoptosis in cancer cells. This combination has been studied in various cancer types including non-small cell lung cancer (NSCLC), prostate cancer, and urothelial cancer.

Brand names
Vandetanib + Taxotere
Other names
docetaxel + ZD6474
02

Targets

EGFR (Epidermal growth factor receptor)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)TUBB (Tubulin (alpha and beta subunits))

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