NL-OMON30517撤回3 期
A phase III, randomized, double-blind, placebo-controlled, multicenter clinical trial of Rebif New Formulation (44 mcg tiw and 44 mcg ow) in subjects at high risk of converting to Multiple Sclerosis - Rebif FLEXible dosing in early Multiple Sclerosis (REFLEX)
Clinical Research Assistance0 个研究点目标入组 25 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 撤回
- 发起方
- 入组人数
- 25
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
- •Subject with a single, first clinical event suggestive of MS within the last 60 days (clock starts 24 hours after onset). The event must be a new neurological abnormality present for at least 24 hours, either mono-polysymptomatic, other than a paresthesia, vegetative or cerebral dysfunction
排除标准
- •Subject has a diagnosis of Multiple Sclerosis ( per Mc Donald creteria 2005)
研究者
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