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首页> 外文期刊>Clinical drug investigation >Effects of prulifloxacin on cardiac repolarization in healthy subjects: a randomized, crossover, double-blind versus placebo, moxifloxacin-controlled study.
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Effects of prulifloxacin on cardiac repolarization in healthy subjects: a randomized, crossover, double-blind versus placebo, moxifloxacin-controlled study.

机译:普利沙星对健康受试者心脏复极的影响:一项随机,交叉,双盲与安慰剂莫西沙星对照研究。

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BACKGROUND AND OBJECTIVE: Prulifloxacin, a broad-spectrum fluoroquinolone, is quantitatively transformed after oral administration into ulifloxacin, the active metabolite. On the basis of preclinical data suggesting that prulifloxacin is not likely to prolong the QT interval, a trial to assess the potential effects of prulifloxacin on QT and corrected QT (QTc) interval in humans was performed. METHODS: Fifty-two healthy subjects were randomized into three groups to receive prulifloxacin 600 mg, moxifloxacin 400mg and placebo once daily for 5 days, using a crossover, double-blind versus placebo, moxifloxacin-controlled study. At baseline and days 1 and 5, three 12-lead digital ECGs were recorded before and up to 24 hours after dosing at nine predefined timepoints. Blood samples were also collected at each treatment timepoint. ECG data were analysed in a blinded manner by a centralized laboratory using skilled readers. QT values were corrected for heart rate using an individual correction method (QTcI) as the primary variable, and Fridericia's method as reference. RESULTS: In forty-eight subjects who completed the study, compared with placebo, prulifloxacin had no relevant effect on cardiac repolarization, with the largest mean QTcI increase being 3.97 ms (one-sided 95% CI 0.01, 7.93), whereas moxifloxacin demonstrated the expected positive effect (maximum mean QTcI increase of 12.0 ms, one-sided 95% CI 8.66, 15.34), thus demonstrating the good sensitivity of the study. A statistically significant correlation between QTcI changes and plasma concentrations was found for moxifloxacin but not for ulifloxacin. CONCLUSION: Prulifloxacin at steady state after therapeutic doses has no significant effects on the QTc interval and thus should prove to have no cardiac liability.
机译:背景与目的:广谱氟喹诺酮普利沙星经口服给药后定量转化为活性代谢物奥利沙星。根据临床前数据表明普利沙星不太可能延长QT间隔,开展了一项试验以评估普利沙星对人的QT和校正后的QT(QTc)间隔的潜在影响。方法:采用交叉,双盲与安慰剂,莫西沙星对照研究,将52例健康受试者随机分为三组,分别接受普鲁沙星600 mg,莫西沙星400mg和安慰剂,连续5天,每天一次。在基线,给药第1天和第5天,在给药前和给药后24小时(共9个预定时间点)记录了三个12导联数字ECG。在每个治疗时间点也采集血样。心电图数据由中央实验室使用熟练的阅读器以盲法分析。使用个体校正方法(QTcI)作为主要变量并以Fridericia方法为参考对心率校正QT值。结果:完成这项研究的48位受试者,与安慰剂相比,普利沙星对心脏复极没有相关影响,最大QTcI升高为3.97 ms(单侧95%CI 0.01,7.93),而莫西沙星表明预期的积极作用(最大平均QTcI增加12.0 ms,单侧95%CI为8.66,15.34),从而证明了该研究的良好敏感性。对于莫西沙星,QTcI变化与血浆浓度之间存在统计学上的显着相关性,而对于奥利沙星则没有。结论:治疗剂量后稳定的普鲁沙星对QTc间隔无明显影响,因此应证明对心脏没有影响。

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