Best practices for the use of itraconazole as a replacement for ketoconazole in drug-drug interaction studies

• Published in: Journal of clinical pharmacology Vol. 56; no. 2; p. 143
• Main Authors: Liu, Lichuan, Bello, Akintunde, Dresser, Mark J, Heald, Donald, Komjathy, Steven Ferenc, O'Mara, Edward, Rogge, Mark, Stoch, S Aubrey, Robertson, Sarah M
• Format: Journal Article
• Language: English
• Published: England 01.02.2016
• Subjects: Antifungal Agents - administration & dosage; Antifungal Agents - pharmacokinetics; Clinical Trials as Topic; Drug Interactions; Humans; Itraconazole - administration & dosage; Itraconazole - pharmacokinetics; Ketoconazole - administration & dosage; Ketoconazole - pharmacokinetics; CYP3A; ketoconazole; itraconazole; drug interaction
• ISSN: 1552-4604
• DOI: 10.1002/jcph.562

Ketoconazole has been widely used as a strong cytochrome P450 (CYP) 3A (CYP3A) inhibitor in drug-drug interaction (DDI) studies. However, the US Food and Drug Administration has recommended limiting the use of ketoconazole to cases in which no alternative therapies exist, and the European Medicines Agency has recommended the suspension of its marketing authorizations because of the potential for serious safety concerns. In this review, the Innovation and Quality in Pharmaceutical Development's Clinical Pharmacology Leadership Group (CPLG) provides a compelling rationale for the use of itraconazole as a replacement for ketoconazole in clinical DDI studies and provides recommendations on the best practices for the use of itraconazole in such studies. Various factors considered in the recommendations include the choice of itraconazole dosage form, administration in the fasted or fed state, the dose and duration of itraconazole administration, the timing of substrate and itraconazole coadministration, and measurement of itraconazole and metabolite plasma concentrations, among others. The CPLG's recommendations are based on careful review of available literature and internal industry experiences.