Richmond Pharmacology Ltd, London, UK.
St George's, University of London, London, UK.
Clin Pharmacol Drug Dev. 2018 Jan;7(1):67-76. doi: 10.1002/cpdd.370. Epub 2017 Aug 1.
A thorough QT/QTc study in healthy white Caucasian subjects demonstrated that rupatadine has no proarrhythmic potential and raised no cardiac safety concerns. The present phase 1 study aimed to confirm the cardiac safety of rupatadine in healthy Japanese subjects. In this randomized, double-blind, placebo-controlled study, 27 healthy Japanese subjects were administered single and multiple escalating rupatadine doses of 10, 20, and 40 mg or placebo. Triplicate electrocardiogram (ECG) recordings were performed on days -1, 1, and 5 at several points, and time-matched pharmacokinetic samples were also collected. Concentration-effect analysis based on the change in the QT interval corrected using Fridericia's formula (QTcF) from average baseline was performed. Data from the formal TQT study in white Caucasian subjects was used for a comparison analysis. The ECG data for rupatadine at doses up to 40 mg did not show an effect on the QTc interval of regulatory concern. The sensitivity of this study to detect small changes in the QTc interval was confirmed by demonstrating a significant shortening of QTcF on days 1 and 5 four hours after a standardized meal. The data from this study exhibited no statistically significant differences in the QTc effect between Japanese and white Caucasian subjects.
一项在健康白种高加索人群中进行的全面 QT/QTc 研究表明,芦帕他定没有致心律失常的潜力,也不会引起心脏安全性问题。本 1 期研究旨在确认芦帕他定在健康日本人群中的心脏安全性。在这项随机、双盲、安慰剂对照研究中,27 名健康日本受试者单次和多次递增服用芦帕他定 10、20 和 40mg 或安慰剂。在几个时间点进行了三次心电图(ECG)记录,并采集了时间匹配的药代动力学样本。基于平均基线校正后的 QT 间期(QTcF)的变化进行基于浓度的效应分析。使用来自白种高加索人群的正式 TQT 研究的数据进行比较分析。在高达 40mg 的芦帕他定剂量下,心电图数据未显示出对 QTc 间隔有监管关注的影响。通过证明在标准餐后 4 小时,第 1 天和第 5 天的 QTcF 明显缩短,证实了该研究对 QTc 间隔微小变化的敏感性。这项研究的数据显示,日本和白种高加索人群之间的 QTc 效应没有统计学上的显著差异。