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临床试验/NCT00616954
NCT00616954终止3 期

An Investigator Initiated, Prospective, Randomized, Controlled Study in Order to Evaluate the Effect of Anti-thymocyte Globulin (Fresenius ATG) on Engraftment, Graft Versus Host Disease (GVHD) and Graft Versus Leukemia (GVL) Effect in Haplo-identical Allogeneic Hematopoietic Stem-cell Transplantation

Hadassah Medical Organization1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2008年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
50
试验地点
1
主要终点
Day of day of neutrophil engraftment (ANC>0.5x10^9/L)

研究概览

简要总结

This study is planned to evaluated whether ATG is needed in haploidentical stem cell transplantation

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
3 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient age 3-70 years old with a disease necessitating allogeneic SCT.
  • Patients must have a mismatched donor willing and capable of donating peripheral blood stem cells and/or bone marrow progenitor cells using conventional techniques, and lymphocytes if indicated (mismatched defined as 3/6-4/6 HLA matching).
  • Each patient / patient's guardian must sign written informed consent.
  • Patients must have an ECOG PS ≤ 2; Creatinine <2.0 mg/dl; Ejection fraction >40%; DLCO >50% of predicted; Serum bilirubin <3 gm/dl; elevated GPT or GOT >3 x normal values.

排除标准

  • Not fulfilling any of the inclusion criteria.
  • Active life-threatening infection.
  • Overt untreated infection.
  • Known hypersensitivity to ATG.
  • HIV seropositivity, Hepatitis B or C antigen positivity with evidence of active hepatitis.
  • Pregnant or lactating women.
  • Donor contraindication (HIV seropositive confirmed by Western Blot Hepatitis B antigenemia; positive HCV antibodies with positive HCV PCR; evidence of bone marrow disease; unable to donate bone marrow or peripheral blood due to concurrent medical condition).
  • Inability to comply with study requirements.

研究组 & 干预措施

1

Experimental

with ATG-F

干预措施: ATG-F (Drug)

结局指标

主要结局

Day of day of neutrophil engraftment (ANC>0.5x10^9/L)

时间窗: 30 days

Day of platelet engraftment >25x10^9/L

时间窗: 30 days

次要结局

  • AGVHD occurrence(100 days)
  • DFS at 100 days(100 days)
  • Day of platelet engraftment >50x10^9/L(100 days)
  • TRM(100 days)
  • TRT(100 days)
  • AGVHD grade(100 days)
  • OS(100 days)
  • Time to AGVHD(100 days)
  • Infections incidence(100 days)

研究者

申办方类型
Other

研究点 (1)

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