Pharmacokinetic interaction between nevirapine and darunavir with low-dose ritonavir in HIV-1-infected patients

被引:9
作者
Sekar, Vanitha [1 ]
Lefebvre, Eric [2 ]
Marien, Kris [3 ]
De Pauw, Martine [3 ]
Vangeneugden, Tony [3 ]
Pozniak, Anton [4 ]
Hoetelmans, Richard M. W. [3 ]
机构
[1] Tibotec Inc, Yardley, PA 19067 USA
[2] Janssen Cilag BV, Tilburg, Netherlands
[3] Tibotec BVBA, Mechelen, Belgium
[4] Chelsea & Westminster Hosp, St Stephens Ctr, London, England
关键词
darunavir; nevirapine; pharmacokinetic interactions; ritonavir; EFFICACY; SAFETY;
D O I
10.1111/j.1365-2125.2009.03430.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
center dot The protease inhibitor (PI) darunavir with low-dose ritonavir (DRV/r) and the non-nucleoside reverse transcriptase inhibitor (NNRTI) nevirapine (NVP) are used in combination with other antiretroviral agents and they may be co-administered for the treatment of HIV-1 infection. center dot There is the potential for a pharmacokinetic interaction between NVP and DRV/r, since these drugs use similar metabolic pathways. WHAT THIS STUDY ADDS center dot This study assesses for the first time the extent of the drug-drug interaction between NVP and DRV/r in the relevant population of HIV-1-infected patients. AIM To investigate the pharmacokinetic interaction between darunavir/ritonavir (DRV/r) and nevirapine (NVP) in 19 HIV-infected patients. METHODS An open-label, randomized, crossover study. Patients received Treatment A [NVP 200 mg b.i.d. plus >= 2 nucleoside/nucleotide reverse transcriptase inhibitors (NRTIs)] and Treatment B [A plus DRV/r 300/100 mg b.i.d. (DRV oral solution)] or Treatment B2 [A plus DRV/r 400/100 mg b.i.d. (DRV tablet)] in two 14-day sessions. RESULTS Mean NVP AUC(12h) increased by 27% [least square means ratio 1.27 (95% confidence interval 1.02, 1.58)]. Mean DRV and ritonavir exposures were similar to historical data. Co-administration was well tolerated. CONCLUSIONS DRV/r and NVP have no clinically relevant interaction. No dose adjustments are required.
引用
收藏
页码:116 / 119
页数:4
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