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

Author:

Zhou Jing1ORCID,Zhang Hong1,Chen Hong1,Zhang George2,Mao John2,Zhang Tianxiang2,Tang Yanan2,Yan Wenhao2,Li Chuanjing2,Ding Yanhua1ORCID,Jin Qinglong3ORCID

Affiliation:

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

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

3. Department of Hepatology, The First Hospital of Jilin University, Jilin, China

Abstract

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 ( n = 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 ( C max ), area under the concentration-time curve up to the last quantifiable time (AUC 0- t ), and area under the plasma concentration-time curve from time 0 extrapolated to infinity (AUC 0-∞ ) 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 ( T max ) and elimination half-life ( T 1/2 ). 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 Trials Registered at ClinicalTrials.gov ( NCT06106113 ).

Funder

The Capital Construction Funds within the provincial budget for 2020

Publisher

American Society for Microbiology

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