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临床试验/NCT01413685
NCT01413685终止4 期

Interest of Calcineurin Activity for the Therapeutic Tacrolimus Monitoring in Renal Recipients

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 23 人开始时间: 2009年1月最近更新:
适应症

试验速览

阶段
4 期
状态
终止
入组人数
23
试验地点
2
主要终点
Determination of tacrolimus concentrations in whole blood and of calcineurin activities in lymphocytes

研究概览

简要总结

The purpose is to define if calcineurin activity is a better biological parameter than blood concentration for the therapeutic tacrolimus monitoring.

详细描述

Some authors showed that the determination of calcineurin (enzyme of cyclosporin and tacrolimus action) activity was very interesting in bone narrow and hepatic transplant in order to monitor tacrolimus or cyclosporin. Indeed, Furthermore, target Tac concentrations still fail to provide in certain patients an appropriate immunosuppression reflected by rejection. Because a lack of data in renal transplant, we propose to study this population treated by tacrolimus, mycophenolate mofetil and corticoids in the first three months following the transplantation.

Our major aim is to study the relationship between calcineurin activity and immunologic events in 200 renal recipients treated with tacrolimus in the first three months following transplant. Immunologic events could be acute rejections and infraclinical rejections. The second aims are 1) if this relationship exists, to define the threshold predicting acute rejection using ROC-curve, 2) to define variations between pharmacodynamic (calcineurin activity) and pharmacokinetic (whole blood concentrations) tacrolimus monitoring and 3) to compare calcineurin activity in patients with acute rejection and those with borderline rejection. Blood samples will be collected into EDTA-containing vacutainers prior to the tacrolimus morning administration and at 2, 4, 6 and 9 hours following the administration at D7, D14 and D21. Whole blood tacrolimus concentrations and calcineurin activity were measured using LCMSMS and HPLC techniques. After D21, only residual measurements will be carried out at D28, M2 and M3. A comparative statistical analysis will be performed between data defined with and without rejection. In case of difference, a ROC curve analysis could define normal ranges of calcineurin activity.

This is the second study of the Sud FRANCILIEN Institute for Research in Nephrology-Transplantation defined with Nephrology departments in Mondor and BICETRE hospitals and the object "Interest of pharmacodynamics of immunosuppressive drugs in renal-transplant recipients" is a new theme of these teams.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Diagnostic
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

  • adult renal transplant recipients
  • treated by tacrolimus (Prograf or ADVAGRAF), corticoids, Cellcept,

排除标准

  • patients with a high risk of bad compliance (toxicomania, severe psychiatric troubles)
  • multiorgan transplant patients with mTOR inhibitors treatments
  • HIV infected patients
  • lack of consent for this study

结局指标

主要结局

Determination of tacrolimus concentrations in whole blood and of calcineurin activities in lymphocytes

时间窗: at day 8, day15, day21 (pharmacokinetics on 4 times samples), day 28, month 2 and month 3 (residual measurement)

次要结局

  • Pharmacogenetics (3A5)(at day 8, day 15, day 21, day 28, month 2 and month 3)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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