跳至主要内容
临床试验/NCT00121810
NCT00121810已完成4 期

An Open Label, Randomized, Multicenter Study to Evaluate the Efficacy and Safety of Early Calcineurin Inhibitor Withdrawal in Recipients of Primary Renal Allografts Maintained Long-term on Mycophenolate Mofetil (MMF) (CellCept®) and Sirolimus (Rapamune®)

Hoffmann-La Roche0 个研究点目标入组 305 人开始时间: 2003年8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
305
主要终点
Mean Percent Change in Glomerular Filtration Rate From Baseline to Month 12

研究概览

简要总结

This 2-arm study recruited kidney transplant patients who were receiving standard care of calcineurin inhibitors (CNIs, tacrolimus or cyclosporine), CellCept (1.0-1.5 g twice daily) and corticosteroids. They were either randomized to continue this regimen, or CNI therapy was discontinued and replaced by sirolimus therapy (in combination with CellCept and corticosteroids). The effect of these 2 regimens on efficacy, safety and kidney function was evaluated. The anticipated time on study treatment was 1-2 years, and the target sample size was 100-500 individuals.

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 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients 18-75 years of age
  • Kidney transplant 30-180 days post-transplantation
  • Receipt of cyclosporine or tacrolimus, CellCept, and corticosteroids for greater than 14 days prior to study entry
  • No known contraindications to sirolimus

排除标准

  • Multiple organ transplant recipients or secondary kidney transplant recipients
  • Corticosteroid-resistant rejection episode within 90 days prior to study entry or corticosteroid-sensitive rejection episode within 30 days prior to study entry
  • More than 1 biopsy-proven episode of acute rejection prior to study entry
  • Treated with sirolimus before the study
  • Organ transplant or expected organ transplant, other than kidney
  • History of malignancy in the last 5 years (except successfully treated localized non-melanotic skin cancer)

研究组 & 干预措施

2

Active Comparator

干预措施: Calcineurin inhibitors (Drug)

1

Experimental

干预措施: mycophenolate mofetil [CellCept] (Drug)

1

Experimental

干预措施: Corticosteroids (Drug)

1

Experimental

干预措施: Sirolimus (Drug)

2

Active Comparator

干预措施: mycophenolate mofetil [CellCept] (Drug)

2

Active Comparator

干预措施: Corticosteroids (Drug)

结局指标

主要结局

Mean Percent Change in Glomerular Filtration Rate From Baseline to Month 12

时间窗: baseline to 12 months

The primary efficacy endpoint was mean percent change in renal function from baseline to 12 months postrandomization, as measured by Glomerular Filtration Rate utilizing renal clearance of cold iothalamate. percent change= \[(Glomerular Filtration Rate at Month 12-Glomerular Filtration Rate at baseline)/Glomerular Filtration Rate at baseline\]\*100 percent.

次要结局

  • Mean Percent Change in Glomerular Filtration Rate From Baseline to Month 24(Baseline to 24 months)
  • Mean Percent Change in Serum Creatinine From Baseline to Months 6, 12, and 24(baseline, 6, 12, and 24 months)
  • Mean Percent Change in Calculated Creatinine Clearance From Baseline to Months 6, 12, and 24(baseline 6, 12, and 24 months)
  • Mean Percent Change in Calculated Glomerular Filtration Rate From Baseline to Months 6, 12, and 24 (Nankivell Equation)(baseline, 6, 12, and 24 months)

研究者

申办方类型
Industry

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