Kakuda Thomas N, Woodfall Brian, De Marez Tine, Peeters Monika, Vandermeulen Kati, Aharchi Fatima, Hoetelmans Richard M W
Janssen Research & Development LLC, Titusville, NJ, USA.
J Antimicrob Chemother. 2014 Mar;69(3):728-34. doi: 10.1093/jac/dkt421. Epub 2013 Oct 23.
Drug-drug interactions between etravirine and rifabutin or clarithromycin were examined in two separate open-label, randomized, two-period, crossover trials in HIV-negative, healthy volunteers.
Rifabutin study: 16 participants received 300 mg of rifabutin once daily (14 days) and then 800 mg of etravirine twice daily (Phase 2 formulation; 21 days) plus 300 mg of rifabutin once daily (days 8-21). Clarithromycin study: 16 participants received 200 mg of etravirine twice daily (commercial formulation; 8 days) and then 500 mg of clarithromycin twice daily (13 days) plus 200 mg of etravirine twice daily (days 6-13). A 14 day washout period between treatments was mandatory in both studies. Full pharmacokinetic profiles of each drug and safety/tolerability were assessed.
Rifabutin decreased etravirine exposure by 37%; etravirine decreased rifabutin and 25-O-desacetyl rifabutin exposure by 17%. Clarithromycin increased etravirine exposure by 42%, whereas etravirine decreased clarithromycin exposure by 39% and increased 14-OH clarithromycin exposure by 21%. No serious adverse events were reported in either trial.
Short-term etravirine coadministration with rifabutin or clarithromycin was well tolerated. Etravirine can be coadministered with 300 mg of rifabutin once daily in the absence of an additional potent cytochrome P450 inducer. No dose adjustments are required upon etravirine/clarithromycin coadministration, but alternatives to clarithromycin are recommended when used for Mycobacterium avium complex prophylaxis or treatment.
在两项针对HIV阴性健康志愿者的独立开放标签、随机、两阶段交叉试验中,研究了依曲韦林与利福布汀或克拉霉素之间的药物相互作用。
利福布汀研究:16名参与者每天一次接受300mg利福布汀(14天),然后每天两次接受800mg依曲韦林(2期制剂;21天)加每天一次300mg利福布汀(第8 - 21天)。克拉霉素研究:16名参与者每天两次接受200mg依曲韦林(市售制剂;8天),然后每天两次接受500mg克拉霉素(13天)加每天两次200mg依曲韦林(第6 - 13天)。两项研究中,治疗之间均必须有14天的洗脱期。评估了每种药物的完整药代动力学特征以及安全性/耐受性。
利福布汀使依曲韦林的暴露量降低了37%;依曲韦林使利福布汀和25 - O - 去乙酰利福布汀的暴露量降低了17%。克拉霉素使依曲韦林的暴露量增加了42%,而依曲韦林使克拉霉素的暴露量降低了39%,并使14 - OH克拉霉素的暴露量增加了21%。两项试验均未报告严重不良事件。
依曲韦林与利福布汀或克拉霉素短期联合给药耐受性良好。在没有额外强效细胞色素P450诱导剂的情况下,依曲韦林可与每天一次300mg利福布汀联合使用。依曲韦林/克拉霉素联合给药时无需调整剂量,但用于鸟分枝杆菌复合体预防或治疗时,建议使用克拉霉素的替代药物。