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临床试验/NCT04088760
NCT04088760终止2 期

Safety and Efficacy of TCRαβ+/CD19+ Depleted Allogeneic Hematopoietic Stem Cell Transplantation for Malignant and Non-malignant Disorders in Children and Adolescent/Young Adult Patients

Children's Hospital Medical Center, Cincinnati1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2019年9月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
15
试验地点
1
主要终点
Incidence of Infusion-related Reactions

研究概览

简要总结

The purpose of this study is to investigate the safety and efficacy of TCRαβ+/CD19+ depleted allogeneic hematopoietic stem cell transplant (HSCT) for malignant and non-malignant disorders in children and adolescent/young adult patients using the CliniMACS® immunomagnetic selection device (Miltenyi Biotec).

详细描述

Acute graft versus host disease (GVHD) remains a significant cause of morbidity and mortality and is the biggest barrier to successful allogeneic hematopoietic cell transplantation (HSCT) outcomes. Improved methods of acute GVHD prevention are needed. TCRαβ+/CD19+ depletion of allogeneic hematopoietic stem cell products offers an opportunity to limit the risk of acute GVHD by removing TCRαβ+ T cells and CD19+ B cells which participate in acute GVHD initiation and perpetuation. The purpose of this study is to investigate the safety and efficacy of TCRαβ+/CD19+ depleted allogeneic hematopoietic stem cell transplant (HSCT) for malignant and non-malignant disorders in children and adolescent/young adult patients using the CliniMACS® immunomagnetic selection device (Miltenyi Biotec).

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

性别
All
接受健康志愿者

入选标准

  • Any patient being treated at Cincinnati Children's Hospital requiring an allogeneic HSCT who lacks an HLA-genotypically matched related donor. Genotypically matched related donors are allowed when there is a clinical desire to avoid the use of GVHD prophylaxis medications.

排除标准

  • Prior allogeneic transplant with active acute or chronic GVHD, or life-threatening infection. Patients with a prior history of allogenic transplant without active GVHD or life-threatening infection can be considered.

研究组 & 干预措施

TCRαβ+/CD19+ depleted HSCT

Experimental

干预措施: TCRαβ+/CD19+ depleted allogeneic hematopoietic stem cell transplant (HSCT) (Drug)

结局指标

主要结局

Incidence of Infusion-related Reactions

时间窗: 100 days

Number of patients who experienced infusion reactions including rash, fever, difficulty breathing, and blood pressure abnormalities at the time of infusion of stem cells.

次要结局

  • Engraftment and Sustained Donor Chimerism(28 days and 1 year)
  • Number of Participants With Acute GVHD(100 days)
  • Number of Participants With Chronic GVHD(1 year)
  • GVHD-free Survival(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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