跳至主要内容
临床试验/NCT01166724
NCT01166724终止3 期

Renal Allograft Function and Histology Following Switching From A Tacrolimus to Sirolimus (SRL)-Based Immunosuppression- Clinical and Mechanistic Impact

The Cleveland Clinic1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2010年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
12
试验地点
1
主要终点
Biopsy-derived Measures of Fibrosis

研究概览

简要总结

The investigators hypothesize that Tacrolimus (Tac) withdrawal from a Tac, MMF and steroid based triple therapy regimen leads to long term improved/stabilized graft function (glomerular filtration rate, GFR) primarily as a consequence of halting CNI-induced fibrogenetic processes that mediate loss of functioning renal tissue. The investigators further hypothesize that the underlying fibrotic mechanism is mediated by pathophysiologic processes that promote epithelial to mesenchymal transition (EMT) (mediated by TGF- ƒÒ) and that early therapeutic intervention may reverse this process (mediated by BMP-7)4.

To address these hypotheses the investigators propose the following clinical and mechanistic aims:

The investigators will test the hypothesis that switching from Tac to SRL in a Tac based triple therapy regimen with MMF and steroids in living and or deceased donor renal transplant recipients leads to improvement in allograft structure and function at 2 years post-transplantation.

The investigators will test this hypothesis in an open label controlled trial where stable renal allograft recipients on Tac, MMF, prednisone maintenance immunosuppression will undergo renal biopsy at 3-4 months post-transplantation and will be randomized to either a) Remain on Tac, MMF and prednisone (CNI-maintenance) or b) switch the Tac to SRL and continue MMF and prednisone. The investigators will then compare biopsy derived measures of allograft fibrosis (CADI, Sirius Red, Banff Chronicity Index) and GFR in the two groups

详细描述

We will test this hypothesis in an open label controlled trial where stable renal allograft recipients on Tac, MMF, prednisone maintenance immunosuppression will undergo renal biopsy at 3-4 months post-transplantation and will be randomized to either a) Remain on Tac, MMF and prednisone (CNI-maintenance) or b) switch the Tac to SRL and continue MMF and prednisone. We will then compare biopsy derived measures of allograft fibrosis (CADI, Sirius Red, Banff Chronicity Index) and GFR in the two groups

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Absence of clinical acute rejection in post-transplant period preceding randomization
  • HLA-mismatched solitary first and second kidney transplant recipients
  • Absence of any degree of rejection (Banff 2007) on renal biopsy at 3-6 months(+/- 2 months) post-transplant.
  • Absence of post-transplant donor-specific antibody

排除标准

  • HLA-identical transplants
  • Contraindication or inability to undergo renal biopsy, like previous complications due to biopsies, anticoagulation, active infection, etc.
  • Positive flow cross match, sensitized recipient, presence of donor-specific antibody.
  • Rejection episode after transplantation, either cellular or humoral on for cause or renal biopsy.
  • Rejection present on pre-randomization renal biopsy.
  • Proteinuria greater than 0.3 gram/day
  • Native kidney disease biopsy proven or likely glomerulonephritis, primary or recurrent FSGS, MPGN or primary or recurrent membranous GN.
  • Hypertriglyceridemia > 400 mg/dL (treated), LDL cholesterol > 160 mg/dL while on optimal treatment.
  • WBC < 2000/mm3, ANC < 1000 mm3, Platelet count < 100,000 mm3
  • Active wound issues.
  • Primary non-function.
  • Active BKV or CMV disease.
  • Evidence of recurrent disease.
  • Active infection
  • Women of childbearing potential unable or unwilling to use birth control during the study.
  • e GFR ≤ 40 ml/ min at screening

研究组 & 干预措施

Sirolimus

Active Comparator

patients will be switched from Tacrolimus to Sirolimus

干预措施: Sirolimus (Drug)

Sirolimus

Active Comparator

patients will be switched from Tacrolimus to Sirolimus

干预措施: Tacrolimus (Drug)

结局指标

主要结局

Biopsy-derived Measures of Fibrosis

时间窗: 12 months

The primary analyses will compare biopsy-derived measures of fibrosis in the Tac-maintenance and SRL groups using the t-test.

次要结局

  • Change in iGFR(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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