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5-羟色胺5-HT6受体拮抗剂HEC30654在健康中国受试者中的安全性、耐受性及药代动力学

Safety, Tolerability and Pharmacokinetics of the Serotonin 5-HT6 Receptor Antagonist, HEC30654, in Healthy Chinese Subjects.

作者信息

Li Xiaojiao, Gao Lei, Liu Jingrui, Zhang Hong, Chen Hong, Yang Lizi, Wu Min, Li Cuiyun, Zhu Xiaoxue, Ding Yanhua, Sun Li

机构信息

Phase I Clinical Trial Unit, The First Hospital of Jilin University, Changchun, China.

Nanguan District Maternal and Child Health and Family Planning Service Center of Changchun, Changchun, China.

出版信息

Front Pharmacol. 2021 Aug 19;12:726536. doi: 10.3389/fphar.2021.726536. eCollection 2021.

Abstract

HEC30654 is a selective 5-HT6 receptor antagonist that was safe and well-tolerated in preclinical models of Alzheimer's disease. The objective of this double-blind, randomized, placebo-controlled clinical trial was to evaluate the safety, tolerability, and pharmacokinetic profile of HEC30654 after single ascending doses in healthy Chinese subjects. Healthy volunteers received a single oral dose of HEC30654 (5, 10, 15, 30, 60 mg). Safety and tolerability assessments included adverse events, vital signs, and findings on electrocardiograms, electroencephalograms, physical examination, and clinical laboratory tests. Pharmacokinetic analysis of HEC30654 and its major metabolite HEC93263 were conducted in blood, urine, and fecal samples. Single doses of HEC30654 up to 30 mg were generally safe and well tolerated, but dose escalation was terminated early as the 60 mg HEC30654 treatment group met the pre-defined stopping rules specified in the protocol. Median t of HEC30654 was 6 h (range, 4-12 h), t of 10-60 mg HEC30654 ranged from 52.1 to 63.8 h. Exposure to HEC30654 across the dose range explored in this study increased more than in proportion to dose. Metabolism of HEC30654 to HEC93263 was slow (<10%), and HEC30654 was mainly eliminated unchanged through feces. Single doses of HEC30654 up to 30 mg were generally safe and well tolerated. Based on preclinical efficacy in various models of cognition, HEC30654 may represent a therapeutic option for symptomatic treatment of cognitive disorders.

摘要

HEC30654是一种选择性5-羟色胺6(5-HT6)受体拮抗剂,在阿尔茨海默病的临床前模型中安全且耐受性良好。这项双盲、随机、安慰剂对照临床试验的目的是评估健康中国受试者单次递增剂量服用HEC30654后的安全性、耐受性和药代动力学特征。健康志愿者口服单次剂量的HEC30654(5、10、15、30、60毫克)。安全性和耐受性评估包括不良事件、生命体征以及心电图、脑电图、体格检查和临床实验室检查结果。对血液、尿液和粪便样本进行了HEC30654及其主要代谢产物HEC93263的药代动力学分析。高达30毫克的单次剂量HEC30654总体上安全且耐受性良好,但由于60毫克HEC30654治疗组符合方案中规定的预先定义的停药规则,剂量递增提前终止。HEC30654的中位达峰时间(t)为6小时(范围为4 - 12小时),10 - 60毫克HEC30654的消除半衰期(t)为52.1至63.8小时。在本研究探索的剂量范围内,HEC30654的暴露量增加幅度超过剂量增加比例。HEC30654代谢为HEC93263的过程缓慢(<10%),HEC30654主要通过粪便以原形排出。高达30毫克的单次剂量HEC30654总体上安全且耐受性良好。基于在各种认知模型中的临床前疗效,HEC30654可能是认知障碍症状性治疗的一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b358/8416768/677cb3458521/fphar-12-726536-g001.jpg

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