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临床试验/NCT01163942
NCT01163942
终止
3 期

A RANDOMIZED CONTROLLED STUDY IN NEWLY DIAGNOSED SEVERE APLASTIC ANEMIA PATIENTS RECEIVING ANTITHYMOCYTE GLOBULIN (ATG), CYCLOSPORIN A, WITH OR WITHOUT G-CSF

European Society for Blood and Marrow Transplantation76 个研究点 分布在 7 个国家目标入组 205 人2001年3月1日

概览

阶段
3 期
干预措施
G-CSF
疾病 / 适应症
Aplastic Anaemia
发起方
European Society for Blood and Marrow Transplantation
入组人数
205
试验地点
76
主要终点
Failure free survival
状态
终止
最后更新
8天前

概览

简要总结

The purpose of this study is to examine the effect of G-CSF on disease free survival and overall survival in aplastic anaemia patients who also receive ATG and Cyclosporin A.

详细描述

Open label, randomized, controlled study of G-CSF, ATG and Cyclosporin A versus ATG and Cyclosporin A. Subjects will be evaluated for hematologic response through day 240. Subjects who do not demonstrate a partial or complete remission by day 120 will be randomized to receive either a second course of ATG or continue their current regimen. Subjects who do demonstrate a partial or complete remission will continue their current regimen through day 240 or maintenance of a complete remission for 30 days. The last day of study treatment will be day 240.

注册库
clinicaltrials.gov
开始日期
2001年3月1日
结束日期
2010年11月1日
最后更新
8天前
研究类型
Interventional
研究设计
Single Group
性别
All

研究者

入排标准

入选标准

  • Severe or very severe aplastic anemia
  • Less than 6 months from diagnosis of severe aplastic anemia by bone marrow biopsy
  • Ethical - Before randomization is done the subject or legally acceptable representative must give written informed consent for participation in the study

排除标准

  • Eligibility for an HLA-matched sibling donor transplant
  • Prior therapy with ATG
  • Cyclosporin A \<4 weeks before enrollment
  • Treatment with G-CSF \<2 weeks before enrollment
  • Other growth factors \<4 weeks before enrollment
  • Diagnosis of Fanconi anemia, dyskeratosis congenita or congenital bone marrow failure syndrome
  • Evidence of myelodysplastic disease
  • Diagnosis or previous history of carcinoma (except local cervical, basal cell, squamous cells, or melanoma)
  • Subjects who have infection, hepatic, renal cardiac, metabolic or other concurrent diseases of such severity that death is imminent
  • Subject is pregnant (e.g. positive HCG test) or is breast feeding

研究组 & 干预措施

Yes G-CSF, No 2nd ATG

Patients randomised to receive G-CSF (alongside ATG and CSA) and to not receive early retreatment in case of no response.

干预措施: G-CSF

Yes G-CSF, Yes 2nd ATG

Patients randomised to receive G-CSF (alongside ATG and CSA) and to receive early retreatment in case of no response.

干预措施: G-CSF

No G-CSF, yes 2nd ATG

Patients randomised not to receive G-CSF (alongside ATG and CSA) but they do receive early retreatment in case of no response.

干预措施: Early retreatment with ATG

Yes G-CSF, No 2nd ATG

Patients randomised to receive G-CSF (alongside ATG and CSA) and to not receive early retreatment in case of no response.

干预措施: Early retreatment with ATG

Yes G-CSF, Yes 2nd ATG

Patients randomised to receive G-CSF (alongside ATG and CSA) and to receive early retreatment in case of no response.

干预措施: Early retreatment with ATG

No G-CSF, No 2nd ATG

Patients randomised not to receive G-CSF (alongside ATG and CSA) and to not receive early retreatment in case of no response.

干预措施: Early retreatment with ATG

No G-CSF, No 2nd ATG

Patients randomised not to receive G-CSF (alongside ATG and CSA) and to not receive early retreatment in case of no response.

干预措施: G-CSF

No G-CSF, yes 2nd ATG

Patients randomised not to receive G-CSF (alongside ATG and CSA) but they do receive early retreatment in case of no response.

干预措施: G-CSF

结局指标

主要结局

Failure free survival

时间窗: day 240

To evaluate the effect of G-CSF on failure free survival and mortality in study subjects also receiving ATG and Cyclosporin A \& time to hematologic response (failure defined as death, non-response or requirement of further treatment).

次要结局

  • Retreatment with ATG(day 240)
  • Safety(6year)
  • Relapse rate(2year)
  • Blood count(day 240)
  • Severity of the disease(day 365)
  • Complete remission(day 120)
  • Severe Infections(day 240)
  • Haematological response(day 240)
  • Benefit of addition of G-CSF(day 240)

研究点 (76)

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