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依曲韦林对HIV阴性志愿者的QT间期及校正QT间期无影响。

Etravirine has no effect on QT and corrected QT interval in HIV-negative volunteers.

作者信息

Peeters Monika, Janssen Katrien, Kakuda Thomas N, Schöller-Gyüre Monika, Lachaert Ruth, Hoetelmans Richard M W, Woodfall Brian, De Smedt Goedele

机构信息

Tibotec BVBA, Mechelen, Belgium.

出版信息

Ann Pharmacother. 2008 Jun;42(6):757-65. doi: 10.1345/aph.1K681. Epub 2008 Apr 29.

Abstract

BACKGROUND

Etravirine (TMC125), a next-generation nonnucleoside reverse transcriptase inhibitor, has shown antiviral efficacy in 2 large Phase 3 trials. In vitro and in vivo studies have shown that etravirine is not associated with proarrhythmic potential. Electrocardiograms (ECGs) from healthy and HIV 1-infected volunteers showed no clinically relevant changes.

OBJECTIVE

To evaluate the effect of 2 etravirine dosing regimens on QT/corrected QT interval (QTc) in HIV-negative volunteers and assess pharmacokinetic and additional safety parameters.

METHODS

A double-blind, double-dummy, randomized, placebo- and active-controlled, 4-period crossover trial was conducted in 41 HIV-negative volunteers. Participants received 4 regimens: etravirine 200 mg twice daily, etravirine 400 mg once daily, moxifloxacin 400 mg once daily (positive control), and placebo in separate 8-day sessions, with each followed by a washout period of 14 or more days. On days -1, 1, and 8 of each session, ECGs were recorded at 11 time points over 12 hours. Pharmacokinetic profiles of etravirine regimens were evaluated and safety was assessed.

RESULTS

Thirty-seven subjects completed the study. For etravirine, the upper limit of the 90% CIs of mean time-matched differences in QTc determined using Fridericia's formula (QTcF) was below 10 msec at all time points, the threshold for prolonged QT as defined by regulatory guidelines. The maximum mean (90% CI) difference of time-matched changes in QTcF versus placebo on day 1 was +0.1 msec (-2.6 to 2.9), -0.2 msec (-2.6 to 2.1), and +10.1 msec (7.3 to 12.8) for etravirine 200 mg twice daily, etravirine 400 mg once daily, and moxifloxacin, respectively. On day 8, these values were +0.6 msec (-2.1 to 3.3), -1.0 msec (-4.4 to 2.5), and +10.3 msec (6.8 to 13.9), respectively. Etravirine produced no clinically significant changes in other ECG parameters. No significant differences between males and females were observed. Both etravirine regimens had similar pharmacokinetic exposure and safety profiles.

CONCLUSIONS

Etravirine does not prolong the QTc interval. No clinically relevant ECG changes were observed in HIV-negative volunteers. Short-term dosing of etravirine in HIV-negative volunteers was generally safe and well tolerated.

摘要

背景

依曲韦林(TMC125)是一种新一代非核苷类逆转录酶抑制剂,已在两项大型3期试验中显示出抗病毒疗效。体外和体内研究表明,依曲韦林与促心律失常的可能性无关。健康志愿者和HIV-1感染志愿者的心电图(ECG)未显示出临床相关变化。

目的

评估两种依曲韦林给药方案对HIV阴性志愿者QT/校正QT间期(QTc)的影响,并评估药代动力学和其他安全性参数。

方法

对41名HIV阴性志愿者进行了一项双盲、双模拟、随机、安慰剂和活性对照的4期交叉试验。参与者接受4种方案:依曲韦林每日2次,每次200mg;依曲韦林每日1次,每次400mg;莫西沙星每日1次,每次400mg(阳性对照);以及安慰剂,各方案为期8天,每个方案后有14天或更长时间的洗脱期。在每个疗程的第-1天、第1天和第8天,在12小时内的11个时间点记录心电图。评估依曲韦林方案的药代动力学特征并评估安全性。

结果

37名受试者完成了研究。对于依曲韦林,使用弗里德里西亚公式(QTcF)确定的QTc平均时间匹配差异的90%CI上限在所有时间点均低于10毫秒,这是监管指南定义的QT延长阈值。在第1天,依曲韦林每日2次,每次200mg、依曲韦林每日1次,每次400mg和莫西沙星与安慰剂相比,QTcF时间匹配变化的最大平均(90%CI)差异分别为+0.1毫秒(-2.6至2.9)、-0.2毫秒(-2.6至2.1)和+10.1毫秒(7.3至12.8)。在第8天,这些值分别为+0.6毫秒(-2.1至3.3)、-1.0毫秒(-4.4至2.5)和+10.3毫秒(6.8至13.9)。依曲韦林在其他心电图参数上未产生临床显著变化。未观察到男性和女性之间的显著差异。两种依曲韦林方案具有相似的药代动力学暴露和安全性特征。

结论

依曲韦林不会延长QTc间期。在HIV阴性志愿者中未观察到临床相关的心电图变化。HIV阴性志愿者短期服用依曲韦林总体上是安全的且耐受性良好。

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