Concentration-QTc Modeling of the DPP-4 Inhibitor HSK7653 in a First-in-Human Study of Chinese Healthy Volunteers

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Xiaoxu Wang, Hongzhong Liu, Cheng Cui, Xiaoye Niu, Haiyan Li, Shu Niu, Pangke Yan, Nan Wu, Fangqiong Li, Qinghe Wu, Kai Chen, Bei Hu, Dongyang Liu
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Abstract

Cofrogliptin (HSK7653) is a long-acting dipeptidyl peptidase-4 inhibitor for the treatment of type 2 diabetes mellitus with a twice-monthly dosing regimen. This study included 62 participants (48 without food effect, 14 with food effect) receiving single doses of HSK7653 (5, 10, 25, 50, 100, and 150 mg) or placebo. Pharmacokinetic samples were collected over 24 hours postdosing and sampling times are aligned with 12-lead electrocardiograms (ECGs) which were derived from continuous ECG recordings. For the concentration-QT interval corrected for heart rate (C-QTc) analysis, we used linear mixed-effects modeling to characterize the correlation between plasma concentrations of HSK7653 and the change from baseline in the QT interval which was corrected by Fridericia's formula (ΔQTcF). The result showed that a placebo-corrected Fridericia corrected QT interval (ΔΔQTcF) prolongation higher than 10 milliseconds is unlikely at the mean maximum observed concentration (Cmax) (411 ng/mL) associated with the recommended therapeutic doses (25 mg twice-monthly), even at the highest supratherapeutic concentration (2425 ng/mL). Thus, HSK7653 does not significantly affect QT prolongation at either recommended doses or the highest supratherapeutic concentration.

DPP-4 抑制剂 HSK7653 在中国健康志愿者首次人体研究中的浓度-QTc 模型。
辅格列汀(HSK7653)是一种长效二肽基肽酶-4抑制剂,用于治疗2型糖尿病,每月给药两次。这项研究包括 62 位参与者(48 位无食物效应,14 位有食物效应),他们接受单剂量 HSK7653(5、10、25、50、100 和 150 毫克)或安慰剂。药代动力学样本在用药后 24 小时内采集,采样时间与 12 导联心电图(ECG)一致,后者来自连续心电图记录。在浓度-QT 间期心率校正(C-QTc)分析中,我们使用线性混合效应模型来描述 HSK7653 血浆浓度与 QT 间期从基线开始的变化之间的相关性,QT 间期从基线开始的变化通过 Fridericia 公式(ΔQTcF)进行校正。结果表明,在与推荐治疗剂量(25 毫克,每月两次)相关的平均最大观察浓度(Cmax)(411 纳克/毫升)下,即使在最高超治疗浓度(2425 纳克/毫升)下,经安慰剂校正的 Fridericia 校正 QT 间期(ΔΔQTcF)延长也不可能超过 10 毫秒。因此,无论是推荐剂量还是最高超治疗浓度,HSK7653 都不会显著影响 QT 延长。
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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