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在中国健康受试者中单剂量和多剂量递增口服给予强效 G 蛋白偶联受体 40(GPR40)激动剂 SHR0534 的耐受性、安全性、药代动力学和药效学。

Tolerability, safety, pharmacokinetics and pharmacodynamics of SHR0534, a potent G protein-coupled receptor 40 (GPR40) agonist, at single- and multiple-ascending oral doses in healthy Chinese subjects.

机构信息

Phase I Clinical Trial Unit, Jiangsu Province Hospital and the First Affiliated Hospital with Nanjing Medical University, Nanjing, China.

Jiangsu Hengrui Medicine Co., Ltd., Lianyungang, China.

出版信息

Xenobiotica. 2021 Mar;51(3):297-306. doi: 10.1080/00498254.2020.1864510. Epub 2020 Dec 28.

DOI:10.1080/00498254.2020.1864510
PMID:33331206
Abstract

SHR0534 is being developed for type-2 diabetes mellitus. Herein the tolerability, safety, pharmacokinetics and pharmacodynamics of SHR0534 in healthy Chinese subjects were assessed in a phase-I, randomized, double-blind, placebo-controlled, single- and multiple-ascending dose study. Forty subjects were randomized 4:1 to receive SHR0534 at the dose of 10, 25, 50 or 100 mg, or placebo, and another eleven subjects were allocated to either the 5 mg group or the placebo group at an 8:3 ratio. All subjects received a single dose on day 1, followed by a 9-day washout and once-daily administrations for 14 consecutive days. Serial samples were collected, and vital signs, electrocardiograms, laboratory tests, urinalysis and adverse events (AEs) were recorded. All doses of SHR0534 were safe and well tolerated with infrequent, generally mild-to-moderate AEs and no serious AEs in the study. SHR0534 was absorbed with a of approximately 4 hours, and systemic exposure increased with dose. Accumulation was minimal (2- to 3-fold) and steady state was reached after seven days of dosing. For pharmacodynamics, no significant hypoglycaemic effects were seen in healthy adults. Good pharmacokinetics and safety were demonstrated but no obvious effect was found.

摘要

SHR0534 正在开发用于 2 型糖尿病。在此,在一项 I 期、随机、双盲、安慰剂对照、单次和多次递增剂量研究中评估了 SHR0534 在健康中国受试者中的耐受性、安全性、药代动力学和药效学。40 名受试者以 4:1 的比例随机分配接受 SHR0534 10、25、50 或 100mg 剂量,或安慰剂,另有 11 名受试者以 8:3 的比例分配至 5mg 组或安慰剂组。所有受试者在第 1 天接受单次给药,随后进行 9 天的洗脱期,然后连续 14 天每天给药一次。采集连续样本,并记录生命体征、心电图、实验室检查、尿液分析和不良事件(AE)。所有 SHR0534 剂量均安全且耐受良好,AE 发生率低,通常为轻至中度,研究中无严重 AE。SHR0534 的吸收半衰期约为 4 小时,且系统暴露随剂量增加而增加。蓄积最小(2-3 倍),给药 7 天后达到稳态。对于药效学,健康成年人未观察到明显的降血糖作用。结果表明,SHR0534 具有良好的药代动力学和安全性,但未发现明显的疗效。

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