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临床试验/NL-OMON51380
NL-OMON51380招募中3 期

A multicenter, international, randomized, placebo controlled, double-blind, parallel group and event driven Phase 3 study of the oral FXIa inhibitor asundexian (BAY 2433334) for the prevention of ischemic stroke in male and female participants aged 18 years and older after an acute non-cardioembolic ischemic stroke or high-risk TIA - OCEANIC-STROKE

Bayer0 个研究点目标入组 105 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
Bayer
入组人数
105

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1. Participants must be >= 18 years of age
  • 2. Acute non-cardioembolic stroke or high-risk TIA
  • 3. Systemic or cerebrovascular atherosclerosis or acute non-lacunar infarct

排除标准

  • 1. Ischemic stroke <= 7 days before the index stroke event
  • 2. Index stroke following procedures or strokes due to other rare causes
  • 3. History of atrial fibrillation/flutter, left ventricular thrombus, mechanic
  • valve or other cardioembolic source of stroke requiring anticoagulation

研究者

发起方
Bayer

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