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Randomized Controlled Trial
. 2009 Feb;53(2):609-14.
doi: 10.1128/AAC.00769-08. Epub 2008 Nov 17.

Drug-drug interaction study of ketoconazole and ritonavir-boosted saquinavir

Affiliations
Randomized Controlled Trial

Drug-drug interaction study of ketoconazole and ritonavir-boosted saquinavir

Benoite Kaeser et al. Antimicrob Agents Chemother. 2009 Feb.

Abstract

Saquinavir, a potent human immunodeficiency virus protease inhibitor, is extensively metabolized by CYP3A4. Saquinavir is coadministered with ritonavir, a strong CYP3A4 inhibitor, to boost its exposure. Ketoconazole is a potent CYP3A inhibitor. The objectives of this study were to investigate the effect of ketoconazole on the pharmacokinetics of saquinavir/ritonavir and vice versa using the approved dosage regimens of saquinavir/ritonavir at 1,000/100 mg twice daily and ketoconazole at 200 mg once daily. This was an open-label, randomized two-arm, one-sequence, two-period crossover study in healthy subjects. In study arm 1, 20 subjects received saquinavir/ritonavir treatment alone for 14 days, followed in combination with ketoconazole treatment for 14 days. In arm 2, 12 subjects received ketoconazole treatment for 6 days, followed in combination with saquinavir/ritonavir treatment for 14 days. The pharmacokinetics were assessed on the last day of each treatment (days 14 and 28 in arm 1 and days 6 and 20 in arm 2). The exposures C(max) and the area under the concentration-time curve from 0 to 12 h (AUC(0-12)) of saquinavir and ritonavir with or without ketoconazole were not substantially altered after 2 weeks of concomitant dosing with ketoconazole. The C(max) and AUC(0-12) of ketoconazole, dosed at 200 mg once daily, were increased by 45% (90% confidence interval = 32 to 59%) and 168% (90% confidence interval = 146 to 193%), respectively, after 2 weeks of concomitant dosing with ritonavir-boosted saquinavir (1,000 mg of saquinavir/100 mg of ritonavir given twice daily). The greater exposure to ketoconazole when given in combination with saquinavir/ritonavir was not associated with unacceptable safety or tolerability. No dose adjustment for saquinavir/ritonavir (1,000/100 mg twice daily) is required when coadministered with 200 mg of ketoconazole once daily, and high doses of ketoconazole (>200 mg/day) are not recommended.

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Figures

FIG. 1.
FIG. 1.
Mean plasma concentration-time profiles of saquinavir (squares) and ritonavir (circles) after 14 days of saquinavir/ritonavir at 1,000/100 mg given twice daily (open symbols, dotted line) and after 14 days of coadministration of saquinavir/ritonavir with ketoconazole at 200 mg once daily (filled symbols, solid line). The standard deviations are shown as error bars.
FIG. 2.
FIG. 2.
Mean plasma concentration-time profiles of ketoconazole after 6 days of ketoconazole at 200 mg given once daily (open symbols, dotted line) and after 14 days of coadministration of ketoconazole with saquinavir/ritonavir at 1,000/100 mg twice daily (filled symbols, solid line). The standard deviations are shown as error bars.

References

    1. Baran, J., Jr., B. Muckatira, and R. Khatib. 2001. Candidemia before and during the fluconazole era: prevalence, type of species and approach to treatment in a tertiary care community hospital. Scand. J. Infect. Dis. 33:137-139. - PubMed
    1. Bjornsson, T. D., J. T. Callaghan, H. J. Einolf, V. Fischer, L. Gan, S. Grimm, J. Kao, S. P. King, G. Miwa, L. Ni, G. Kumar, J. McLeod, S. R. Obach, S. Roberts, A. Roe, A. Shah, F. Snikeris, J. T. Sullivan, D. Tweedie, J. M. Vega, J. Walsh, and S. A. Wrighton. 2003. The conduct of in vitro and in vivo drug-drug interaction studies: a PhRMA perspective. J. Clin. Pharmacol. 43:443-469. - PubMed
    1. Gerber, J. G. 2000. Using pharmacokinetics to optimize antiretroviral drug-drug interactions in the treatment of human immunodeficiency virus infection. Clin. Infect. Dis. 30(Suppl. 2):S123-S129. - PubMed
    1. Khaliq, Y., K. Gallicano, S. Venance, S. Kravick, and D. W. Cameron. 2000. Effect of ketoconazole on RTV and SQV concentrations in plasma and cerebrovascular fluid from patients infected with human immunodeficiency virus. Clin. Pharmacol. Ther. 68:637-646. - PubMed
    1. U.S. Food and Drug Administration. 1999. Guidance for industry—in vivo drug metabolism/drug interaction studies: study design, data analysis, and recommendations for dosing and labeling. U.S. Food and Drug Administration, Center for Drug Evaluation and Research, Center for Biologics Evaluation and Research, Washington, DC. http://www.fda.gov/cder/guidance/index.htm.

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