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临床试验/NCT01706471
NCT01706471已完成4 期

Safety and Efficacy of the Early Introduction of Everolimus (Certican®) With Low Dose of Cyclosporine in de Novo Kidney Recipients After 1 Month of Transplantation

Yonsei University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
60
试验地点
1
主要终点
Reduced Exposure Cyclosporine in Renal Transplant Recipients

研究概览

简要总结

Calcineurin inhibitors, such as cyclosporine and tacrolimus, have improved allograft survival in kidney organ transplantation. Indeed, they have reduced the incidence of acute rejection episodes of cadaveric allograft recipients. Although marked progression has been made in initial survival rates, long-term kidney graft survival has yet to show such encouraging results. Because CNIs are associated with adverse effects, particularly nephrotoxicity, which contribute to declining organ function and eventual graft loss. In kidney transplants, progressive allograft dysfunction has been shown to develop in as many as 94% of patients by 1 year.

Therefore, reducing or eliminating the dose of CNIs to minimize nephrotoxicity must be balanced against the maintenance of adequate immunosuppression.

Certican allows CNI dose reduction then provides renal function improvement and current PSI strategy point out that early intervention is important in managing the risk of CAN before it develops in both de novo and maintenance renal transplant recipients.

To demonstrate Certican early introduction after 1 month provides better renal function with no change of efficacy compared to standard regimen, and also prevent delayed wound healing.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males or Females aged 18~65 years
  • De novo recipients of cadaveric, living unrelated or living related donor kidney transplants
  • Received kidney transplant from aged 10~65years donor
  • Willing to provide written informed consent
  • Completing study visits according to study protocol

排除标准

  • Recipients of multiple organ transplants
  • Kidney transplant from non-heart beating cadaveric donor / organ donor after cardiac death
  • Recipients of A-B-O incompatible transplants or lymphocyte cross-match positive transplants
  • Recipients of extra-renal solid organ transplants or stem cell transplants
  • Recipient/ donor who are known to have anti-HCV, HIV or HBsAg positive
  • Diagnosed as Cancer within the past 5 years (except complete recovered squamous cell or basal cell skin cancer)
  • Drug Hypersensitivity to investigational drugs or related drugs Females are pregnant and lactating
  • Any of the following laboratory abnormalities at screening:
  • ALT, AST, ALP, total bilirubin > 3 times the upper limit
  • ANC < 1,500mm3 or WBC < 2,500mm3 or platelet < 100,000 mm3
  • Cholesterol > 350 mg/dl or 9.0 mmol/L, TG > 500 mg/dl or 5.6mmol/L

研究组 & 干预措施

Everolimus + Low dose CsA +PD

Experimental

干预措施: Everolimus + Low dose CsA +PD (Drug)

Myfortic+ Standard CsA + PD

Active Comparator

干预措施: Myfortic+ Standard CsA + PD (Drug)

结局指标

主要结局

Reduced Exposure Cyclosporine in Renal Transplant Recipients

时间窗: 12 months after the time of kidney transplantation

A 12-month, multi center, randomized, open-label, non-inferiority study of efficacy and safety comparing early introduction of Certican® after 1 month and standard regimen in de novo renal transplant recipients

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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