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临床试验/NCT01794663
NCT01794663已完成2 期

A Three-Part, Multi-Centre, Randomised, Double-Blind, Placebo-Controlled, Parallel-Group, Sequential Adaptive, Phase II Study to Evaluate the Safety, Tolerability and Efficacy of OPN-305, a Humanised Monoclonal Antibody That Blocks Toll-Like Receptor 2, in Renal Transplant Patients at High Risk of Delayed Graft Function

Opsona Therapeutics Ltd.1 个研究点 分布在 1 个国家目标入组 252 人开始时间: 2012年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
252
试验地点
1
主要终点
Measure of Early Graft Function EGF

研究概览

简要总结

When a patient receives a kidney transplant particularly if the kidney is from an older donor or one who has had the kidney removed after their heart has stopped, there is a risk that the newly transplanted kidney may not function immediately. If the delay in function means that dialysis is needed in the first 7 days after the transplantation then this is known as delayed graft function or dDGF. Also delayed graft function that does not require dialysis but is present because the serum creatinine does not fall sufficiently is known as functional delayed graft function or fDGF. This problem is often due to an excessive inflammatory reaction to not having had a blood supply between the time of donation and transplant.

OPN-305 is a monoclonal antibody that blocks Toll-like Receptor 2 which is thought to be partly responsible for increasing the risk of this inflammation. It is hoped that the effects of the inflammation will be reduced and therefore prevent dDGF and fDGF from occurring.

The purpose of the study is to explore how effective OPN-305 is in preventing dDGF and fDGF as well as improving other measures of kidney function and the overall safety of the antibody. In the first part of the study, each patient received an Infusion of one of three possible doses of OPN-305 or a placebo and in the second part the most suitable dose of OPN-305 and a placebo would be used. The purpose of this second part of the study is to find out if a dose of OPN-305 which has already been tested in an earlier part of this study can prevent kidney graft dysfunction. For the purposes of this study, kidney function will be assessed using the composite of delayed graft function (dDGF) because dialysis is necessary in the first 7 days and functional delayed graft function that does not require dialysis but is present because the serum creatinine, a key measure of renal function, does not fall sufficiently (fDGF) in the first 7 days post-transplant.

Protocol OPN305-103 follows out to 12 months post-transplant the clinical status and graft function of patients who have completed the 6-month post-transplant period under Part A or Part B of OPN305-102.

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
Double (Participant, 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

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

OPN-305

Experimental

干预措施: OPN-305 (Drug)

Matching placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Measure of Early Graft Function EGF

时间窗: First 7 days following renal transplantation

Initiation of dialysis in the first 7 days following renal transplantation and failure of serum creatinine to decrease by at least 10% daily on 3 successive days during the first week post transplantation

次要结局

  • Number of Adverse events (AEs)(6 months)
  • Reason for subsequent readmissions(6 months)
  • Creatinine at 7 and 14 days and at 1, 3 and 6 months(7 and 14 days and at 1, 3 and 6 months)
  • Cystatin C at 7 and 14 days and at 1, 3 and 6 months(7 and 14 days and at 1, 3 and 6 months)
  • Symmetrical dimethylarginine at 7 and 14 days and at 1, 3 and 6 months(7 and 14 days and at 1, 3 and 6 months)
  • Incidence of slow graft function(5 days post-transplant)
  • Serum creatinine over time(over the duration of follow-up)
  • Composite endpoint(6 months)
  • Time to biopsy-proven kidney allograft rejection(6 months)
  • Time to first dialysis or functional delayed graft function and delayed graft function duration(30 days)
  • Blood and urine biomarkers for acute kidney injury (AKI)(days 2, 7, 14, 28, 90 and 180)
  • Duration of initial hospitalization(6 months)
  • Duration of subsequent readmissions(6 months)
  • Nature of Adverse events (AEs)(6 months)
  • Rate of primary non-function (permanent lack of function of the allograft)(6 months)
  • Number of dialysis sessions between 0 and 30 days post-transplantation(30 days)
  • Incidence of infections(6 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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