Nelonemdaz for Patients With Acute Ischemic Stroke Undergoing Endovascular Reperfusion Therapy: A Randomized Phase II Trial

医学 改良兰金量表 安慰剂 冲程(发动机) 随机化 随机对照试验 优势比 临床终点 内科学 外科 麻醉 缺血 缺血性中风 病理 替代医学 工程类 机械工程
作者
Ji Man Hong,Jin Soo Lee,Yeong-Bae Lee,Dong Hoon Shin,Dong‐Ick Shin,Younghun Hwang,Seong Hwan Ahn,Jae Guk Kim,Sung Il Sohn,Sun U. Kwon,Ji Sung Lee,Byoung Joo Gwag,Ángel Chamorro,Dennis W. Choi,Ángel Chammorro,Eung Yeop Kim,Jin Wook Choi,Min-Ju Yeo,Jin Ho Kwak,Sung Eun Lee,Jeong‐Ho Hong,Sang Kil Lee,Yoon-Joo Lee,Min-Joo Lee
出处
期刊:Stroke [Ovid Technologies (Wolters Kluwer)]
卷期号:53 (11): 3250-3259 被引量:7
标识
DOI:10.1161/strokeaha.122.039649
摘要

Nelonemdaz is a multitarget neuroprotectant that selectively blocks N-methyl-D-aspartate receptors and scavenges free radicals, as proven in preclinical ischemia-reperfusion studies. We aimed to evaluate the safety and efficacy of nelonemdaz in patients with acute ischemic stroke receiving endovascular reperfusion therapy.This phase II randomized trial involved participants with large-artery occlusion in the anterior circulation at baseline who received endovascular reperfusion therapy <8 hours from symptom onset at 7 referral stroke centers in South Korea between October 29, 2016, and June 1, 2020. Two hundred thirteen patients were screened and 209 patients were randomly assigned at a 1:1:1 ratio using a computer-generated randomization system. Patients were divided into 3 groups based on the medication received-placebo, low-dose (2750 mg) nelonemdaz, and high-dose (5250 mg) nelonemdaz. The primary outcome was the proportion of patients with modified Rankin Scale scores of 0-2 at 12 weeks.Two hundred eight patients were assigned to the placebo (n=70), low-dose (n=71), and high-dose (n=67) groups. The groups had similar baseline characteristics. The primary outcome was achieved in 183 patients, and it did not differ among the groups (33/61 [54.1%], 40/65 [61.5%], and 36/57 [63.2%] patients; P=0.5578). The common odds ratio (90% CI) indicating a favorable shift in the modified Rankin Scale scores at 12 weeks was 1.55 (0.92-2.60) between the placebo and low-dose groups and 1.61 (0.94-2.76) between the placebo and high-dose groups. No serious adverse events were reported.The study arms showed no significant difference in the proportion of patients achieving modified Rankin Scale scores of 0-2 at 12 weeks. Nevertheless, nelonemdaz-treated patients showed a favorable tendency toward achieving these scores at 12 weeks, without serious adverse effects. Thus, a large-scale phase III trial is warranted.URL: https://clinicaltrials.gov; Unique identifier: NCT02831088.
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