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临床试验/EUCTR2013-001150-10-GB
EUCTR2013-001150-10-GB进行中(未招募)1 期

A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, MULTI-CENTER TRIAL TO EVALUATE THE SAFETY AND EFFICACY OF ECULIZUMAB IN PATIENTS WITH RELAPSING NEUROMYELITIS OPTICA (NMO)

Alexion Pharmaceuticals, Inc.0 个研究点目标入组 143 人开始时间: 2013年7月25日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
143

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Male or female patient = 18 years old
  • - Diagnosis of NMO or NMO spectrum disorder
  • - NMO-IgG seropositive
  • - Historical Relapse of at least 2 relapses in the last 12 months or 3 relapses in the last 24 months, with at least 1 relapse in the 12 months prior to the Screening
  • - EDSS score =7
  • - Immunosuppressive therapy is allowed provided patients have been on a stable maintenance dose prior to the Screening and remain on a stable dose for the duration of the study
  • - Patients must be willing and able to give written informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 119
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 13

排除标准

  • - Use of rituximab or mitoxantrone within 3 months prior to Screening
  • - Use of IVIg within 3 weeks prior to screening

研究者

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