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利奈唑胺标准治疗剂量和超治疗剂量对 QTc 间期延长无影响。

Lack of an effect of standard and supratherapeutic doses of linezolid on QTc interval prolongation.

机构信息

Pfizer, Inc., 235 East 42nd St., New York, NY 10017, USA.

出版信息

Antimicrob Agents Chemother. 2011 Sep;55(9):4302-7. doi: 10.1128/AAC.01723-10. Epub 2011 Jun 27.

Abstract

A double-blind, placebo-controlled, four-way crossover study was conducted in 40 subjects to assess the effect of linezolid on corrected QT (QTc) interval prolongation. Time-matched, placebo-corrected QT intervals were determined predose and at 0.5, 1 (end of infusion), 2, 4, 8, 12, and 24 h after intravenous dosing of linezolid 600 and 1,200 mg. Oral moxifloxacin at 400 mg was used as an active control. The pharmacokinetic profile of linezolid was also evaluated. At each time point, the upper bound of the 90% confidence interval (CI) for placebo-corrected QTcF values (i.e., QTc values adjusted for ventricular rate using the correction methods of Fridericia) for linezolid 600 and 1,200-mg doses were <10 ms, which indicates an absence of clinically significant QTc prolongation. At 2 and 4 h after the moxifloxacin dose, corresponding to the population T(max), the lower bound of the two-sided 90% CI for QTcF when comparing moxifloxacin to placebo was >5 ms, indicating that the study was adequately sensitive to assess QTc prolongation. The pharmacokinetic profile of linezolid at 600 mg was consistent with previous observations. Systemic exposure to linezolid increased in a slightly more than dose-proportional manner at supratherapeutic doses, but the degree of nonlinearity was small. At a supratherapeutic single dose of 1,200 mg of linezolid, no treatment-related increase in adverse events was seen compared to 600 mg of linezolid, and no clinically meaningful effects on vital signs and safety laboratory evaluations were noted.

摘要

一项在 40 例受试者中进行的双盲、安慰剂对照、四交叉研究评估了利奈唑胺对校正 QT(QTc)间期延长的影响。在静脉给予利奈唑胺 600mg 和 1200mg 后,分别在给药前、0.5、1(输注结束时)、2、4、8、12 和 24 小时测定时间匹配的、安慰剂校正的 QT 间期。口服莫西沙星 400mg 作为活性对照。还评估了利奈唑胺的药代动力学特征。在每个时间点,利奈唑胺 600mg 和 1200mg 剂量的安慰剂校正 QTcF 值(即使用 Fridericia 校正方法校正心室率的 QTc 值)的 90%置信区间(CI)上限均<10ms,表明没有临床意义的 QTc 延长。在莫西沙星剂量后 2 和 4 小时,相当于群体 T(max),比较莫西沙星和安慰剂时 QTcF 的双侧 90%CI 的下限>5ms,表明该研究足以评估 QTc 延长。利奈唑胺的药代动力学特征与之前的观察结果一致。在治疗剂量下,利奈唑胺的系统暴露量以略高于剂量比例的方式增加,呈轻度非线性,但非线性程度较小。在利奈唑胺 1200mg 的超治疗剂量单剂量下,与 600mg 的利奈唑胺相比,未见与治疗相关的不良事件增加,且对生命体征和安全实验室评估无临床意义的影响。

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