Drug intelligence / Profile preview

vandetanib-eluting radiopaque beads

Development stage
Unknown
Lead developer
Bio-Technology General
Modality
Small Molecules
Administration
Intra-arterial
01

Overview

BTG-002814 is a novel drug delivery system consisting of vandetanib-eluting radiopaque beads designed for transarterial chemoembolization (TACE) in liver cancer patients. It contains 100 mg of vandetanib loaded onto tiny radiopaque beads. When injected into the hepatic artery, these beads lodge in blood vessels feeding the tumor, blocking blood flow and releasing vandetanib directly into the tumor microenvironment. The radiopaque nature of the beads allows physicians to visualize their distribution using CT scans, enabling more precise delivery and treatment monitoring. Vandetanib itself is a multi-targeted tyrosine kinase inhibitor that acts as a RET inhibitor, VEGFR-2 inhibitor, and EGFR antagonist. These mechanisms allow vandetanib to target both angiogenesis (blood vessel formation) and direct cancer cell growth, even in hypoxic (low-oxygen) conditions.

Other names
vandetanib-eluting radiopaque embolic beads
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR3 (Vascular endothelial growth factor receptor 3)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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