Development of a Multi-Purpose Comprehensive Physiologically Based Pharmacokinetic Model for Crizotinib: An Example...

Crizotinib exhibits a complex drug-drug interaction as it is a CYP3A4 substrate and acts as both a time-dependent inhibitor and inducer of the enzyme. Absorption of crizotinib is also complex as it exhibits a prolonged absorption phase. The primary objective of this research was to develop a comprehensive physiologically based pharmacokinetic (PBPK) model to mechanistically describe both metabolism and absorption of crizotinib. The established crizotinib adult PBPK model was extrapolated to pediatric population using the modified CYP3A4 ontogeny profile to evaluate the pharmacokinetic (PK) profile after a single dose administration of crizotinib under the fasted condition in pediatric population age between 1 to 6 years old. The model was further applied to conduct virtual bioequivalence (BE) trials including clinically observed intra-subject coefficient of variation (ICV%) in both adult and pediatric populations. In adult subjects, the estimated geometric mean ratio for AUC_inf and C_max for oral solution (OS) vs granules formulation was 98.33 and 89.94, respectively with probability of demonstrating BE in adults of 100% for AUC_inf and 90.3% for C_max. In pediatric subjects, the probability of demonstrating BE success was 99.7% for both AUC_inf and C_max. The high probability of BE was replicated with the assumed higher ICV of 29% in pediatrics for both AUCinf and C_max. The granules (commercial formulation) can be considered BE to OS (Phase 3 clinical formulation) in adults, as well as pediatric subjects aged between 1 to 6 years old.