NL-OMON32595已完成2 期
A randomised, double-blind, placebo-controlled, multiple-dose, dose-escalation study of the safety, tolerability, and pharmacokinetics of Lu AA24493 in patients with acute ischemic stroke - CEPO multiple-dose study 12053A
undbeck0 个研究点目标入组 6 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 6
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
- •Male or female patients, aged 50-90 years; clinical diagnosis of acute ischemic stroke; measurable stroke-related deficit at the start of treatment; stable condition; treatment can be initiated 0-48 hours after onset of stroke symptoms; acceptance of hospital stay of at least 120 hours after first IMP dose (for full inclusion criteria refer to study protocol, page 28)
排除标准
- •Treatment with a thrombolytic within the previous 24 hours; previous treatment with erythropoietin of Lu AA24493; score >0 on the NIHSS consciousness item; pre-stroke mRS score >1, indicating previous disability; uncontrolled hypertension; history or imaging evidence of various CNS abnormalities (for further details, and full exclusion criteria, refer to study protocol, page 28)
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