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临床试验/NCT01222039
NCT01222039已完成1 期

Multicenter Clinical Trial Phase I/II Randomized, Controlled, for the Evaluation of Safety and Feasibility of Therapy With Two Different Doses of Allogenic Mesenchymal Stem Cells From Adipose Tissue in Patients With Chronic Graft Versus Host Disease.

Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud8 个研究点 分布在 1 个国家目标入组 19 人开始时间: 2010年6月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
19
试验地点
8
主要终点
Number of adverse events

研究概览

简要总结

The main purpose of this trial is to assess the safety and feasibility of treatment with two-dose infusion of allogeneic mesenchymal stem cells from adipose tissue expanded in vitro in patients undergoing haematopoietic stem cell transplantation (HSCT, who have developed chronic and extensive graft versus host disease (GVHD).

Mesenchymal stem cells (MSCs) express low levels of HLA class I molecules, and do not express class II molecules neither CD40, CD80 and CD86, being unable to induce proliferation of allogeneic lymphocytes. In addition, MSCs inhibit lymphocyte proliferation by inhibiting cell division and maintaining these cells in a quiescent state. This supports the hypothesis that MSCs are universal suppressors.

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

  • Patients who develop chronic extensive GVHD as determined by the National Institute of Health Consensus Development Project on Criteria for Clinical Trials in Chronic GVHD (Biol Blood Marrow Transplant 2005; 11: 945-955), and which meet the following criteria:
  • They have never received therapy for chronic GVHD.
  • They have de novo or quiescent chronic extended GVHD.

排除标准

  • Concomitant severe systemic infection.
  • Oncologic or hematological condition relapse.
  • Estimated life expectancy less than 1 week.
  • Patients who do not give their informed consent.

结局指标

主要结局

Number of adverse events

时间窗: 24 months

次要结局

  • Percentage of patients in each group that may potentially reduce corticosteroids at week 7, 20 and 42, started immunosuppressive treatment and percentage of patients at week 56 have been suspended on full immunosuppressive treatment(12 months)
  • Overall survival and disease-free survival.(12 months)
  • Changes in lymphocyte subsets and levels of inflammatory and antiinflammatory cytokines in each of the groups.(12 months)

研究者

发起方
Andalusian Initiative for Advanced Therapies - Fundación Pública Andaluza Progreso y Salud
申办方类型
Other
责任方
Sponsor

研究点 (8)

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