Drug intelligence / Profile preview

vandetanib + omeprazole

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

Overview

vandetanib + omeprazole describes the co-administration of two drugs: vandetanib, a *small molecule tyrosine kinase inhibitor* approved for the treatment of medullary thyroid cancer, and omeprazole, a widely used *proton pump inhibitor* for gastric acid-related disorders. Vandetanib inhibits key signaling pathways involved in tumor angiogenesis and growth, specifically acting on vascular endothelial growth factor receptor-2 (VEGFR-2), epidermal growth factor receptor (EGFR), and rearranged during transfection (RET) tyrosine kinases. Omeprazole reduces gastric acid secretion by irreversibly inhibiting the H+/K+ ATPase (proton pump) in gastric parietal cells. Pharmacokinetic studies indicate that concurrent administration of vandetanib and omeprazole does not result in clinically significant drug-drug interactions. Vandetanib exposure (AUC) remains unchanged when combined with omeprazole, and neither drug requires dose adjustment when co-administered. The combination is generally well tolerated, though standard pharmacovigilance, including ECG monitoring for QT prolongation (related to vandetanib), should be practiced. No synergistic therapeutic intent is implied; this is not an approved fixed-dose combination, but reflects concomitant use, often due to supportive care (e.g., acid suppression) during vandetanib therapy[1][2][3].

Other names
vandetanib + omeprazole
02

Targets

PTK6 (Protein-tyrosine kinase 6)ATP4A (Potassium–transporting ATPase alpha chain 1)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)EGFR T790M (Epidermal growth factor receptor T790M mutant)VEGFR2 (Vascular endothelial growth factor receptor 2)TEK (Angiopoietin-1 receptor)RET (Rearranged during transfection receptor tyrosine kinase)

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