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在肝功能受损和正常的中国受试者中,新型 3CL 蛋白酶抑制剂 GST-HG171 的药代动力学和安全性。

Pharmacokinetics and safety of GST-HG171, a novel 3CL protease inhibitor, in Chinese subjects with impaired and normal liver function.

机构信息

Phase I Clinical Research Center, The First Hospital of Jilin University, Jilin, China.

Fujian Akeylink Biotechnology Co., Ltd., Fuzhou, Fujian, China.

出版信息

Antimicrob Agents Chemother. 2024 Aug 7;68(8):e0053924. doi: 10.1128/aac.00539-24. Epub 2024 Jul 11.

Abstract

GST-HG171 is a potent, broad-spectrum, orally bioavailable small-molecule 3C-like (3CL) protease inhibitor that was recently approved for treating mild to moderate coronavirus disease 2019 patients in China. Since cytochrome P450 (CYP) enzymes, primarily CYP3A, are the main metabolic enzymes of GST-HG171, hepatic impairment may affect its pharmacokinetic (PK) profile. Aiming to guide clinical dosing for patients with hepatic impairment, this study, using a non-randomized, open-label, single-dose design, assessed the impact of hepatic impairment on the PK, safety, and tolerability of GST-HG171. Patients with mild and moderate hepatic impairment along with healthy subjects were enrolled ( = 8 each), receiving a single oral dose of 150 mg GST-HG171, with concurrent administration of 100 mg ritonavir to sustain CYP3A inhibition before and after GST-HG171 administration (-12, 0, 12, and 24 hours). Compared to subjects with normal hepatic function, the geometric least-squares mean ratios (90% confidence intervals) for GST-HG171's maximum plasma concentration (), area under the concentration-time curve up to the last quantifiable time (AUC), and area under the plasma concentration-time curve from time 0 extrapolated to infinity (AUC) in subjects with mild hepatic impairment were 1.14 (0.99, 1.31), 1.07 (0.88, 1.30), and 1.07 (0.88, 1.29), respectively. For moderate hepatic impairment, the ratios were 0.87 (0.70, 1.07), 0.82 (0.61, 1.10), and 0.82 (0.61, 1.10), respectively. Hepatic impairment did not significantly alter GST-HG171's peak time () and elimination half-life (). GST-HG171 exhibited good safety and tolerability in the study. Taken together, mild to moderate hepatic impairment minimally impacted GST-HG171 exposure, suggesting no need to adjust GST-HG171 dosage for patients with mild to moderate hepatic impairment in the clinic.Clinical TrialsRegistered at ClinicalTrials.gov (NCT06106113).

摘要

GST-HG171 是一种有效的、广谱的、口服生物可利用的 3C 样(3CL)蛋白酶抑制剂,最近在中国被批准用于治疗轻度至中度 2019 年冠状病毒病患者。由于细胞色素 P450(CYP)酶主要是 CYP3A,是 GST-HG171 的主要代谢酶,因此肝损伤可能会影响其药代动力学(PK)特征。为了指导肝损伤患者的临床给药,本研究采用非随机、开放标签、单次剂量设计,评估了肝损伤对 GST-HG171 的 PK、安全性和耐受性的影响。共纳入轻度和中度肝损伤患者和健康受试者(各 8 例),单次口服 GST-HG171 150mg,同时给予 100mg 利托那韦,在 GST-HG171 给药前(-12、0、12 和 24 小时)和之后持续抑制 CYP3A。与肝功能正常的受试者相比,轻度肝损伤受试者 GST-HG171 的最大血浆浓度()、浓度-时间曲线下面积直至最后可定量时间(AUC)和从 0 时间外推至无穷大的血浆浓度-时间曲线下面积(AUC)的几何均数比值(90%置信区间)分别为 1.14(0.99,1.31)、1.07(0.88,1.30)和 1.07(0.88,1.29)。对于中度肝损伤,比值分别为 0.87(0.70,1.07)、0.82(0.61,1.10)和 0.82(0.61,1.10)。肝损伤并未显著改变 GST-HG171 的达峰时间()和消除半衰期()。在本研究中,GST-HG171 表现出良好的安全性和耐受性。总的来说,轻度至中度肝损伤对 GST-HG171 的暴露影响较小,提示在临床上无需调整轻度至中度肝损伤患者的 GST-HG171 剂量。临床试验在 ClinicalTrials.gov 注册(NCT06106113)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32ef/11304707/9f3c43d62b94/aac.00539-24.f001.jpg

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