Optimization of Drug-Drug Interaction Study Design: Comparison of Minimal Physiologically Based Pharmacokinetic Models on Prediction of CYP3A Inhibition by Ketoconazole

Author:

Han Bing,Mao Jialin,Chien Jenny Y.,Hall Stephen D.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference23 articles.

1. STOCHASTIC PREDICTION OF CYP3A-MEDIATED INHIBITION OF MIDAZOLAM CLEARANCE BY KETOCONAZOLE

2. Comparison of midazolam and simvastatin as cytochrome P450 3A probes

3. Oral administration of a low dose of midazolam (75 microg) as an in vivo probe for CYP3A activity;Eap;Eur J Clin Pharmacol,2004

4. Einolf HJ (2007) Comparison of different approaches to predict metabolic drug-drug interactions. Xenobiotica 37:1257–1294.

5. FDA (2012) Drug Interaction Studies —Study Design, Data Analysis, Implications for Dosing, and Labeling Recommendations. http://wwwfdagov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM292362pdf .

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