Lack of Concentration-QTc Relationship and Cardiac Risk With Vatiquinone Therapeutic and Supratherapeutic Doses

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Lucy Lee, Stephen Flach, Hongqi Xue, Lavanya Arivelu, Lee Golden, Ronald Kong, Borje Darpo
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Abstract

Vatiquinone, a 15-lipoxygenase inhibitor, is in development for patients with Friedreich ataxia. The study determined the effect of vatiquinone on electrocardiogram parameters. This was a 2-part, single-center, randomized, double-blinded, and placebo-controlled study. Part 1 used an adaptive approach to identify a supratherapeutic dose, while Part 2 evaluated the effect of vatiquinone on Fridericia corrected QT interval (QTcF). A safe and tolerated supratherapeutic dose of 1400 mg was identified. Concentration-QTcF analysis confirmed there was no statistically significant relationship between vatiquinone concentration and QTcF. QTcF effect (ie, ΔΔQTcF) exceeding 10 milliseconds was excluded for concentrations up to approximately 11,500 ng/mL. By-time-point analysis confirmed that least-squares mean ΔΔQTcF was below 10 milliseconds. Largest least-squares mean ΔΔQTcF of 1.5 milliseconds was observed at 2 hours after dosing. Vatiquinone did not have a clinically relevant effect on heart rate nor on cardiac conduction (PR interval and QRS interval). No new safety signals were found, as safety data are consistent with the known safety profile of vatiquinone. These findings altogether demonstrated that there is a minimal cardiac risk for vatiquinone concentrations up to the supratherapeutic dose level.

Abstract Image

瓦替喹酮治疗剂量和超治疗剂量缺乏浓度-QTc 关系和心脏病风险。
瓦替醌是一种15-脂氧合酶抑制剂,目前正在开发用于治疗弗里德里希共济失调症患者的药物。该研究确定了瓦替醌对心电图参数的影响。这是一项由两部分组成的单中心、随机、双盲和安慰剂对照研究。第一部分采用适应性方法确定超治疗剂量,第二部分评估了伐替喹酮对弗里德里希校正QT间期(QTcF)的影响。最终确定的安全耐受超治疗剂量为 1400 毫克。浓度-QTcF 分析证实,瓦替醌浓度与 QTcF 之间没有统计学意义上的显著关系。浓度最高约为 11,500 纳克/毫升时,QTcF 影响(即 ΔΔQTcF)超过 10 毫秒的情况被排除在外。分时点分析证实,最小二乘平均值 ΔΔQTcF 低于 10 毫秒。用药 2 小时后观察到的最大最小平方平均值 ΔΔQTcF 为 1.5 毫秒。瓦替喹酮对心率和心脏传导(PR 间期和 QRS 间期)均无临床相关影响。没有发现新的安全性信号,因为安全性数据与已知的瓦替喹酮安全性特征一致。这些研究结果表明,瓦替醌浓度达到超治疗剂量水平时,对心脏造成的风险极小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
10.00%
发文量
154
期刊介绍: Clinical Pharmacology in Drug Development is an international, peer-reviewed, online publication focused on publishing high-quality clinical pharmacology studies in drug development which are primarily (but not exclusively) performed in early development phases in healthy subjects.
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