Safety and tolerability of Rinvecalinase Alfa (DM199) for acute ischemic stroke (ReMEDy1).

IF 6.9 2区 医学 Q1 CLINICAL NEUROLOGY
International Journal of Stroke Pub Date : 2026-07-01 Epub Date: 2025-11-06 DOI:10.1177/17474930251396480
Bruce Cv Campbell, Scott E Kasner, Annette D Lista, John J Volpi, Timothy J Kleinig, Dennis Cordato, Helen M Dewey, Philip Mc Choi, Carlos Garcia-Esperon, Ramesh Sahathevan, Tissa Wijeratne, Andrew A Wong, Darshan Ghia, Geoffrey C Cloud, Michael Giuffre, Philip M Bath
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引用次数: 0

Abstract

Background: Rinvecalinase alfa (DM199), a recombinant form of human tissue kallikrein-1 (KLK1), aims to promote local vasodilation to ischemic brain and enhance collateral blood flow. The ReMEDy1 trial tested the safety and tolerability of rinvecalinase alfa in ischemic stroke.

Methods: ReMEDy1 was a phase II, randomized, double-blind, placebo-controlled, study conducted at 13 Australian sites. Ninety-two patients with NIH Stroke Scale (NIHSS) 6-25 were enrolled within 24 h of ischemic stroke onset. Patients were randomized 1:1 to receive rinvecalinase alfa (1 µg/kg intravenous infusion followed by 3 µg/kg subcutaneously every 3 days for 22 days) or placebo. The primary outcome was safety, assessed by adverse events (AEs) and serious adverse events (SAEs). Secondary outcomes included changes in NIHSS, modified Rankin Scale (mRS), and Barthel Index (BI) at Days 22 and 90. Post hoc analyses excluded patients who underwent endovascular therapy (EVT).

Results: The median age was 72, NIHSS 10, and onset-to-randomization was 19.5 h. SAEs were reported in 20/47 (43.5%) rinvecalinase alfa patients and 14/45 (31.1%) placebo patients. Most patients experienced at least one AE; the most common in the rinvecalinase alfa group were constipation (60.9%), oral candidiasis (23.9%), and nausea (17.4%). Stroke-in-evolution by Day 90 occurred in 0 (0%) rinvecalinase alfa patients versus 6 (13.3%) placebo patients; 4/6 (66.7%) placebo patients with stroke-in-evolution died. No significant differences were observed in secondary efficacy outcomes at Day 90. Post hoc analyses in patients not treated with EVT suggested a tendency toward improved excellent global outcomes with rinvecalinase alfa.

Conclusions: Rinvecalinase alfa appeared to be safe and generally well-tolerated in ischemic stroke patients, with potential efficacy in reducing stroke progression. Further studies are needed to confirm efficacy and long-term benefits in patients without EVT.

Registrations: https://www.

Clinicaltrials: gov/study/NCT03290560.

Rinvecalinase Alfa (DM199)治疗急性缺血性卒中的安全性和耐受性(remey1)。
drinvecalinase alfa (DM199)是一种重组人组织钾likrein-1 (KLK1),旨在促进局部缺血脑血管舒张,增强侧支血流量。ReMEDy1试验测试了rinvecalinase alfa在缺血性卒中中的安全性和耐受性。remedy1是一项在澳大利亚13个地点进行的随机、双盲、安慰剂对照的II期研究。入选92例符合NIH卒中量表(NIHSS) 6-25的缺血性卒中发病24小时内患者。患者以1:1的比例随机分配,接受rinvecalinase alfa(静脉输注1µg/kg,随后每3天皮下注射3µg/kg,共22天)或安慰剂。主要结局是安全性,通过不良事件(ae)和严重不良事件(sae)来评估。次要结局包括第22天和第90天NIHSS、改良Rankin量表(mRS)和Barthel指数(BI)的变化。事后分析排除了接受血管内治疗(EVT)的患者。结果中位年龄为72岁,NIHSS为10岁,发病至随机化时间为19.5h。有20/47(43.5%)的rinvecalinase α患者和14/45(31.1%)的安慰剂患者报告了SAEs。大多数患者至少经历一次AE;rinvecalinase alfa组最常见的是便秘(60.9%)、口腔念珠菌病(23.9%)和恶心(17.4%)。到第90天发生进化中中风的患者为0例(0%),安慰剂患者为6例(13.3%);4/6(66.7%)安慰剂患者死亡。在第90天的次要疗效结果中没有观察到显著差异。在未接受EVT治疗的患者中进行的事后分析表明,rinvecalinase alfa有改善良好的总体结果的趋势。结论:在缺血性脑卒中患者中,曲钙化酶是安全且耐受性良好的,具有降低脑卒中进展的潜在疗效。需要进一步的研究来证实无evt患者的疗效和长期获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Stroke
International Journal of Stroke 医学-外周血管病
CiteScore
13.90
自引率
6.00%
发文量
132
审稿时长
6-12 weeks
期刊介绍: The International Journal of Stroke is a welcome addition to the international stroke journal landscape in that it concentrates on the clinical aspects of stroke with basic science contributions in areas of clinical interest. Reviews of current topics are broadly based to encompass not only recent advances of global interest but also those which may be more important in certain regions and the journal regularly features items of news interest from all parts of the world. To facilitate the international nature of the journal, our Associate Editors from Europe, Asia, North America and South America coordinate segments of the journal.
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