Drug intelligence / Profile preview

vandetanib + docetaxel + prednisolone

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

Overview

This is a **combination regimen** consisting of vandetanib, docetaxel, and prednisolone, studied primarily in the context of metastatic hormone-refractory (castration-resistant) prostate cancer. Vandetanib is a small-molecule oral tyrosine kinase inhibitor that selectively targets vascular endothelial growth factor receptor (VEGFR), epidermal growth factor receptor (EGFR), and rearranged during transfection (RET) signaling, thereby inhibiting angiogenesis and tumor cell proliferation. Docetaxel is a chemotherapy agent that stabilizes microtubules and inhibits cell division. Prednisolone is a synthetic corticosteroid with anti-inflammatory and immunosuppressive properties. The combination was evaluated in Phase II clinical trials, but did not show benefit over placebo plus docetaxel/prednisolone in this indication[1][3].

02

Targets

BCL-2 (BCL-2 family)GR (Glucocorticoid receptor)TUBB (Tubulin (alpha and beta subunits))KCNH2 (Voltage-gated potassium channel subfamily H member 2)VEGFR-1 (Vascular endothelial growth factor receptor 1)PTK6 (Protein-tyrosine kinase 6)VEGFR3 (Vascular endothelial growth factor receptor 3)EGFR T790M (Epidermal growth factor receptor T790M mutant)VEGFR2 (Vascular endothelial growth factor receptor 2)RET (Rearranged during transfection receptor tyrosine kinase)

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