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临床试验/NCT01403389
NCT01403389终止2 期

Pilot Study of the Clinical Activity of Eculizumab for Prevention of Delayed Graft Function in Patients Undergoing Deceased Donor Kidney Transplantation

Schroppel, Bernd, M.D.1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2011年12月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
8
试验地点
1
主要终点
Composite of Delayed Graft Function and Slow Graft Function

研究概览

简要总结

The purpose of this study is to determine if Eculizumab is safe and effective in the prevention of delayed graft function following deceased donor kidney transplantation.

详细描述

Based on experimental data and supportive observations in humans associating complement gene upregulation with ischemic reperfusion injury, it is hypothesized that C5 cleavage is a key step in the pathogenesis of ischemic reperfusion injury following transplantation. It is further hypothesized that eculizumab, an antibody that blocks C5 cleavage in humans will be an effective prophylactic agent to prevent ischemic reperfusion injury in high risk recipients. To test this hypothesis, this study is a pilot prospective, randomized study to test the efficacy of eculizumab vs. placebo given once at the time of transplantation in preventing delayed graft function in first adult recipients of deceased donor kidneys.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 18 or older
  • Weight > 40 kg
  • Male or Female
  • Recipients of first deceased donor kidneys
  • Able to provide written informed consent
  • Transplant candidate as per site specific guidelines
  • Dialysis dependent renal failure (initiated more than 2 months prior to transplant)
  • Novartis Delayed Graft Function Score 3-8
  • Extended criteria donor with brain death, or standard criteria donor with cold ischemic time < 24 hours

排除标准

  • Planned to receive multi-organ transplant
  • Kidneys from donors < 6 years of age
  • Dual kidney transplant (from same donor, including en bloc)
  • Living donor kidney
  • Highly sensitized recipients (PRA > 50%)
  • Previous transplant
  • Participation in another investigational trial
  • Recipient BMI > 40
  • ABO incompatible
  • DCD Donor
  • Preemptive kidney transplant
  • Recipients with DGF scores < 3 or > 8
  • Women who are pregnant or breast feeding
  • Women of child bearing potential who are unable or unwilling to use a medically acceptable form of contraception
  • Patients infected with HIV, HCV or HBV
  • Active bacterial or other infection which is clinically significant in the opinion of the investigator
  • Patients with history of splenectomy
  • Patients with history of meningococcal disease
  • Patients with known or suspected hereditary complement deficiency
  • Patients with history of cancer (other than non-melanoma skin cancers) within the last 5 years

研究组 & 干预措施

Eculizumab

Experimental

干预措施: Eculizumab (Drug)

0.9% Sodium Chloride

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Composite of Delayed Graft Function and Slow Graft Function

时间窗: Up to 6 months

Delayed Graft Function defined as follows: 1. A need for at least one dialysis treatment during the first 7 days after transplantation (not including a single session for hyperkalemia or hypervolemia in the first 48 hours) 2. A less than or equal to 50% reduction in serum creatinine in the first 24 hours post-transplantation 3. A serum creatinine reduction ratio \< 30% at 48 hours post-transplantation Slow Graft Function Defined as Follows: A functioning graft at Day 5 Post-transplantation with a serum creatinine \> 3 mg/dL and no need for dialysis

次要结局

未报告次要终点

研究者

发起方
Schroppel, Bernd, M.D.
申办方类型
Indiv
责任方
Sponsor

研究点 (1)

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