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临床试验/EUCTR2010-019631-35-IT
EUCTR2010-019631-35-IT进行中(未招募)1 期

AN OPEN-LABEL, SINGLE-ARM,MULTICENTER TRIAL TO DETERMINE SAFETY AND EFFICACY OF ECULIZUMAB IN THE PREVENTION OF ANTIBODY MEDIATED REJECTION (AMR) IN SENSITIZED RECIPIENTS OF A KIDNEY TRANSPLANT FROM A DECEASED DONOR

ALEXION PHARMACEUTICALS0 个研究点目标入组 40 人开始时间: 2012年6月8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
40

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

  • 1. Male or female patients =18 years old 2. Patients with Stave V chronic kidney disease who will recieve a kindney transplant from a deceased donor to whom they are sensitized 3. Patients must be able to understand the informed consent form and willing to comply with study procedures
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 40
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 0

排除标准

  • 1. has received treatment with eculizumab at any time prior to enrolling in this study 2. ABO incompatible with deceased donor

研究者

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