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评估依鲁替尼对心脏复极的影响。

Evaluation of Eluxadoline Effect on Cardiac Repolarization.

机构信息

Lodestar Pharma Consulting, LLC, Durham, NC, USA.

PPD, Austin, TX, USA.

出版信息

Clin Pharmacol Drug Dev. 2018 Sep;7(7):727-736. doi: 10.1002/cpdd.453. Epub 2018 Apr 16.

Abstract

This study evaluated the effects of eluxadoline, a mixed μ-opioid receptor (OR) and κ-OR agonist and δ-OR antagonist, on cardiac repolarization. This evaluator-blinded, placebo- and positive-controlled, 4-period crossover study randomized healthy men and women to single oral doses of eluxadoline (therapeutic dose 100 mg or supratherapeutic dose 1000 mg), moxifloxacin 400 mg, or placebo. QT data were corrected using individual custom correction (QTcI). The primary endpoint was the change from baseline in QTcI intervals (ΔQTcI) between eluxadoline and placebo (ΔΔQTcI). An upper bound of the 95% confidence interval around ΔΔQTcI of 10 milliseconds was considered clinically significant. Concentration-QTc data were analyzed using a repeated-measures, mixed-effects linear model. Sixty-four volunteers were treated, and 58 completed the study. Assay sensitivity was demonstrated with moxifloxacin (noted by ΔΔQTcI of 11.94 milliseconds). The maximum ΔΔQTcI for eluxadoline 1000 mg was 4.10 milliseconds 1 hour postdose (1-sided 95% upper confidence bound, 5.81 milliseconds), and for eluxadoline 100 mg was 1.20 milliseconds at 0.5 hours postdose (1-sided 95% upper confidence bound, 2.91 milliseconds). Primary ΔΔQTcI results were confirmed using Fridericia's formula for QTc. Categorical, morphological, and concentration-QTc analyses were consistent with the primary and secondary findings. There were no significant gender effects on ΔΔQTcI values. The most common adverse events were contact dermatitis and nausea (12.5% each) and dizziness (10.9%); adverse events were more frequent in the eluxadoline 1000 mg group. In conclusion, eluxadoline, at therapeutic or supratherapeutic doses, did not significantly prolong QT intervals, and was safe and generally well tolerated in this study population.

摘要

这项研究评估了混合 μ 阿片受体(OR)和 κ-OR 激动剂以及 δ-OR 拮抗剂埃卢索多林对心脏复极的影响。这是一项评估员设盲、安慰剂和阳性对照、四周期交叉研究,将健康男性和女性随机分为单次口服埃卢索多林(治疗剂量 100 毫克或超治疗剂量 1000 毫克)、莫西沙星 400 毫克或安慰剂。QT 数据采用个体定制校正(QTcI)校正。主要终点是埃卢索多林与安慰剂相比(ΔΔQTcI)的 QTcI 间期变化(ΔQTcI)。ΔΔQTcI 的 95%置信区间上限为 10 毫秒被认为具有临床意义。采用重复测量、混合效应线性模型分析浓度-QTc 数据。64 名志愿者接受了治疗,58 名志愿者完成了研究。莫西沙星证明了检测灵敏度(ΔΔQTcI 为 11.94 毫秒)。埃卢索多林 1000 毫克的最大 ΔΔQTcI 为 1 小时后 4.10 毫秒(单侧 95%置信上限为 5.81 毫秒),而埃卢索多林 100 毫克在 0.5 小时后为 1.20 毫秒(单侧 95%置信上限为 2.91 毫秒)。主要 ΔΔQTcI 结果使用 Fridericia 公式 QTc 进行了确认。分类、形态和浓度-QTc 分析与主要和次要发现一致。ΔΔQTcI 值无显著性别差异。最常见的不良事件是接触性皮炎和恶心(各 12.5%)和头晕(10.9%);埃卢索多林 1000 毫克组的不良事件更为频繁。总之,在治疗剂量或超治疗剂量下,埃卢索多林不会显著延长 QT 间期,在本研究人群中安全且一般耐受良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8061/6175186/f6126683d365/CPDD-7-727-g001.jpg

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