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临床试验/NCT01549665
NCT01549665Unknown1 期

Umbilical Cord Blood-derived Mesenchymal Stem Cells for the Treatment of Steroid-refractory Acute or Chronic Graft-versus-host-disease

Samsung Medical Center2 个研究点 分布在 2 个国家目标入组 30 人开始时间: 2012年1月1日最近更新:
适应症

试验速览

阶段
1 期
入组人数
30
试验地点
2
主要终点
Safety of UCB-MSC in SR-GVHD

研究概览

简要总结

Graft-versus-host-disease (GVHD) is a major complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT) which may cause acute life-threatening morbidity or chronic disabilities. Although corticosteroid, the primary agent to treat GVHD, may be effective for some patients, outcomes of those who are refractory to corticosteroid are dismal. Secondary agents can be used for steroid-refractory cases; however, their efficacy is variable and usually limited. The quality of life issue of chronic GVHD is especially important for pediatric survivors who have longer life expectancy than adults. Many in-vitro and in-vivo data support immunoregulatory properties of mesenchymal stem cells(MSCs)and possibilities of treating diseases caused by immune dysregulation such as GVHD. Recent data revealed that bone marrow-derived MSCs were very useful to treat steroid-refractory acute GVHD, which led to improved overall survival compared with controls. More recently, a number of reports suggest MSCs may also be useful in treating chronic GVHD as well as acute GVHD. It has been also reported that third party MSCs are also useful as well as those from autologous or HLA-matched donors. The investigator recently demonstrated that MSCs obtained from umbilical cord blood (UCB) have similar immunosuppressive properties as bone marrow-MSCs. UCB-MSCs can be obtained without doing any harm to donors that it may be more appropriate source of MSCs than bone marrow for off-the-shelf use. However, little is known about the safety and efficacy of UCB-MSCs in treating GVHD. Therefore, the investigator designed this study to evaluate the safety and efficacy of UCB-MSCs in treating pediatric patients with steroid-refractory acute or chronic GVHD.

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
1 Day 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Steroid-refractory acute or chronic graft-versus-host-disease
  • Acquisition of consent form
  • 0-30 years of age

排除标准

  • Withdrawal from the study
  • Progression of underlying hematologic diseases
  • Severe adverse effects related to the investigational drug

结局指标

主要结局

Safety of UCB-MSC in SR-GVHD

时间窗: 180 days

* Vital sign * Physical examination * ECOG performance status * Mixed Lymphocyte Reaction(MLR) * Adverse effects related to infusion

次要结局

  • Complete, Partial Response Rate at 28 and 180 Days in participants with SR-GVHD treated with UCB-MSC(180 Days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hong Hoe Koo

MD, PhD

Samsung Medical Center

研究点 (2)

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