Drug intelligence / Profile preview

cediranib + docetaxel

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

Overview

Cediranib + docetaxel is an investigational combination therapy evaluated primarily for the treatment of advanced solid tumors, including metastatic castration-resistant prostate cancer. Cediranib is an oral, potent inhibitor of all three vascular endothelial growth factor receptors (VEGFR-1, -2, and -3), thereby inhibiting tumor angiogenesis. Docetaxel is a well-established chemotherapeutic agent (a taxane) that disrupts microtubule function, resulting in cell cycle arrest and apoptosis. The combination aims to exploit both antiangiogenic (cediranib) and cytotoxic (docetaxel) mechanisms for enhanced antitumor efficacy. Clinical data to date suggest limited additional benefit over docetaxel alone with an increased risk of toxicity, especially in the treatment of metastatic castration-resistant prostate cancer.

Other names
cediranib maleate + docetaxel
02

Targets

TUBB (Tubulin (alpha and beta subunits))VEGFR2 (Vascular endothelial growth factor receptor 2)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)

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