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奈非那韦标准剂量和超治疗剂量对心脏复极化的影响:一项全面的QT研究。

Effects of standard and supratherapeutic doses of nelfinavir on cardiac repolarization: a thorough QT study.

作者信息

Damle Bharat, Fosser Cecilia, Ito Kaori, Tran Anh, Clax Pamela, Uderman Howard, Glue Paul

机构信息

Pfizer Global Research & Development, Pfizer Inc, 685 Third Ave., 685/13/55, New York, NY 10017, USA.

出版信息

J Clin Pharmacol. 2009 Mar;49(3):291-300. doi: 10.1177/0091270008329551.

Abstract

This was a randomized, 4-way crossover, third-party-blinded study in 68 healthy subjects to assess the effect of nelfinavir on QTc interval. Treatments included (A) nelfinavir 1250 mg every 12 hours on days 1-4, (B) nelfinavir 1250 mg every 12 hours on days 1-3 plus 3125 mg on day 4, (C) placebo, and (D) moxifloxacin 400 mg every 24 hours on days 1-4. Pharmacokinetics and triplicate 12-lead electrocardiograms were performed over 12 hours on days 1 and 4. Time-matched, placebo-subtracted, baseline-adjusted changes in QT intervals with Fridericia's (QTcF) correction were determined following nelfinavir and moxifloxacin administration. Neither dose of nelfinavir had a clinically relevant effect on the QTcF interval on day 4 (primary endpoint) and day 1 because at every time point the upper 90% confidence limit was below 10 milliseconds and, furthermore, the mean difference was below 5 milliseconds. Additionally, there was no clinically relevant effect on QTcB (Bazett's correction), uncorrected QT, or the RR interval on days 1 or 4. Pharmacokinetics confirmed adequate systemic exposure to nelfinavir and moxifloxacin. While nelfinavir exposure was higher in poor compared with extensive metabolizers of CYP2C19 isozyme, there were no corresponding significant differences in QTcF change from placebo. At clinically relevant, doses nelfinavir is unlikely to cause QTc prolongation.

摘要

这是一项针对68名健康受试者的随机、四臂交叉、第三方盲法研究,旨在评估奈非那韦对QTc间期的影响。治疗方案包括:(A) 在第1 - 4天每12小时服用1250毫克奈非那韦;(B) 在第1 - 3天每12小时服用1250毫克奈非那韦,并在第4天服用3125毫克;(C) 安慰剂;(D) 在第1 - 4天每24小时服用400毫克莫西沙星。在第1天和第4天的12小时内进行了药代动力学研究和一式三份的12导联心电图检查。在服用奈非那韦和莫西沙星后,确定了采用弗里德里西亚校正法(QTcF)校正的QT间期的时间匹配、减去安慰剂、基线调整后的变化。两种剂量的奈非那韦在第4天(主要终点)和第1天对QTcF间期均无临床相关影响,因为在每个时间点,90%置信区间上限均低于10毫秒,此外,平均差异低于5毫秒。此外,在第1天或第4天,对QTcB(巴泽特校正法)、未校正的QT或RR间期均无临床相关影响。药代动力学证实奈非那韦和莫西沙星有足够的全身暴露。虽然与CYP2C19同工酶的广泛代谢者相比,奈非那韦在代谢不良者中的暴露量更高,但与安慰剂相比,QTcF变化并无相应的显著差异。在临床相关剂量下,奈非那韦不太可能导致QTc延长。

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