Publication | Closed Access

A Mechanistic Physiologically Based Pharmacokinetic-Enzyme Turnover Model Involving both Intestine and Liver to Predict CYP3A Induction-Mediated Drug–Drug Interactions

Systems PharmacologyPharmacokinetic ModelingBiochemistryPharmacological StudyMedicinePhysiologyMechanistic PhysiologicallyPharmacotherapyDrug AbsorptionPharmacologyPhysiologically-based Pharmacokinetic ModelingPharmacokineticsPharmacodynamic Modeling