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人尿激肽释放酶原治疗急性缺血性中风患者:来自一项随机双盲安慰剂对照IIb期和III期临床试验的汇总数据分析

Human urinary kallidinogenase in treating acute ischemic stroke patients: analyses of pooled data from a randomized double-blind placebo-controlled phase IIb and phase III clinical trial.

作者信息

Dong Yi, Qu Jiazhi, Zhang Zhijun, Wang Changjun, Dong Qiang

机构信息

Department of Neurology, Huashan Hospital Affiliated to Fudan University, Shanghai, China.

Department of Medical Affairs, Techpool Bio-Pharma Co., LTD, Chengdu, China.

出版信息

Neurol Res. 2020 Apr;42(4):286-290. doi: 10.1080/01616412.2020.1711648. Epub 2020 Mar 6.

DOI:10.1080/01616412.2020.1711648
PMID:32138624
Abstract

: Intravenous thrombolysis and thrombectomy are recommended for patients whose stroke onsets are within first 6 h, and very few options are available for patients whose stroke onset is more than 6 h, which includes most ischemic stroke patients. Human urinary kallidinogenase (HUK) showed potential clinical benefits in acute ischemic stroke patients. This study aims to investigate the safety and clinical benefits of HUK in ischemic stroke patients.: Patients were recruited for a multicenter double-blind, placebo-controlled phase II b and phase III trial. Neurophysiological outcomes were assessed by the European Stroke Scale (ESS) and the functional outcomes were assessed by the activity of daily living scale (ADL). Safety was monitored by recording adverse events.: The improvements in ESS scores and ADL scores in the HUK group were significantly greater than that in patients receiving placebo. Furthermore, HUK treatment was also associated with a lower rate of disable, according to ADL. HUK-related adverse events occurred at a low rate, in 1.73% of HUK-treated patients.: HUK is safe and provides potential clinical benefits as a treatment for acute ischemic stroke. Further large post-marketing observational studies are needed.

摘要

对于卒中发作在最初6小时内的患者,推荐进行静脉溶栓和取栓治疗,而对于卒中发作超过6小时的患者(其中包括大多数缺血性卒中患者),可用的治疗选择非常少。人尿激肽原酶(HUK)在急性缺血性卒中患者中显示出潜在的临床益处。本研究旨在探讨HUK在缺血性卒中患者中的安全性和临床益处。

患者被招募参加一项多中心双盲、安慰剂对照的IIb期和III期试验。通过欧洲卒中量表(ESS)评估神经生理结果,通过日常生活活动量表(ADL)评估功能结果。通过记录不良事件来监测安全性。

HUK组的ESS评分和ADL评分改善显著大于接受安慰剂治疗的患者。此外,根据ADL,HUK治疗还与较低的致残率相关。HUK相关不良事件发生率较低,在接受HUK治疗的患者中为1.73%。

HUK作为急性缺血性卒中的一种治疗方法是安全的,并具有潜在的临床益处。还需要进一步开展大规模的上市后观察性研究。

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