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临床试验/NCT02129881
NCT02129881已完成1 期

The ONE Study: A Unified Approach to Evaluating Cellular Immunotherapy in Solid Organ Transplantation

Guy's and St Thomas' NHS Foundation Trust4 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2014年4月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
15
试验地点
4
主要终点
Incidence of biopsy-confirmed acute rejection.

研究概览

简要总结

A study to assess cell therapy as a treatment to prevent kidney transplant rejection. The trial will involve purification of naturally occurring regulatory T cells (nTregs) from living-donor renal transplant recipients. The cells will then be grown in the laboratory and re-infused into the patient five days after the kidney transplant. This trial is part of an international European Union funded consortium aimed at evaluating cellular immunotherapy in solid organ transplantation (The ONE Study). It is anticipated that immune regulation induced by nTreg therapy can eventually be used to recude the need for conventional immunosuppression in transplant recipients.

详细描述

Decades of immunosuppressive drug development has produced an array of powerful pharmacological agents, but the various drawbacks with these treatments leaves considerable room for improvement. By harnessing the power of suppressive mechanisms in the human immune system, regulatory cell therapy may be able to support peripheral tolerance and induce a level of donor-specific unresponsiveness that allows for a reduction in the use of conventional immunosuppression in organ transplant recipients. Several alternative regulatory cell types have been identified as potential adjunct immunotherapies for solid organ transplantation and are now approaching a stage of development that would allow clinical testing in an early-stage trial. The EU-funded international ONE study consortium aims to answer the question as to whether Treg treatment, or other immunoregulatory cell-based therapies, can be advanced in the clinical management of solid organ transplant recipients. This particular Treg trial aims to explored the potential of Treg therapy as an adjunct immunosuppressive treatment in living-donor renal transplant recipients through a clinical protocol design shared by other investigators in the ONE study group testing additional regulatory cell therapies in seperate trials.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Incidence of biopsy-confirmed acute rejection.

时间窗: 60 weeks

次要结局

  • Incidence of chronic graft dysfunction(60 weeks)
  • Severity of acute rejection episodes(60 weeks)
  • Incidence of adverse drug reactions(60 weeks)
  • Total immunosuppressive burden(60 weeks)
  • Incidence of neoplasia.(60 weeks)
  • Incidence of graft loss through rejection(60 weeks)
  • Incidence of major and/or opportunistic infections(60 weeks)
  • Time to first acute rejection episode(60 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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