跳至主要内容
临床试验/NCT00472433
NCT00472433终止2 期

A Phase II Study of Alemtuzumab in Autoimmune Cytopenias

Phramongkutklao College of Medicine and Hospital2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2007年3月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
30
试验地点
2
主要终点
To investigate the efficacy of alemtuzumab in terms of objective response rate (ORR: complete remission [CR], partial remission [PR]), progression free survival (PFS), and relapse rate in patients with autoimmune cytopenias

研究概览

简要总结

The majority of cases of autoimmune cytopenias, which includes immune thrombocytopenia (ITP), autoimmune hemolytic anemia, autoimmune neutropenia (AIN) and pure red cell aplasia, will respond to conventional immunosuppressive therapy with or without splenectomy. There is, however, a group of patients with refractory or chronically relapsing autoimmune cytopenias causing life-threatening hemorrhages, infections or anemia. Further problems include the short- and long-term side-effects of corticosteroids, and the potential toxicity of immunosuppressive and cytotoxic agents. An alternative and less toxic approach in these patients may be the treatment with Campath-1H, a humanized IgG monoclonal antibody specific for the CD52 antigen and present on human lymphocytes and monocytes. The main effect of Campath-1H is on T cell and it results in a prolonged and profound depletion of the CD4 and CD8 subpopulations, particularly the CD4 population, and this might "reset" the immune system without the need for total immune ablation.Therefore, this study is designed to investigate safety and efficacy of repeated Campath treatment cycles in autoimmune cytopenia.In order to minimize possible side effects of accumulating Campath, the 3 treatment cycles will be administered in consecutively reduced doses.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients must have a diagnosis of the following autoimmune cytopenias:
  • immune thromobocytopenia purpura (ITP) autoimmune hemolytic anemia (AIHA) autoimmune neutropenia (AIN) pure red cell aplasia (PRCA) and
  • Patients must have refractory disease according to the following criteria
  • not respond to steroids or
  • need prednisolone more than 15 mg/d for maintenance therapy
  • Complete work up for baseline evaluation and measurement
  • Age > 18 years
  • Patient's free written inform consent

排除标准

  • Patients with a known hypersensitivity to murine proteins or to any component of alemtuzumab
  • Patients with poor performance status (ECOG criteria of 3-4)
  • Serologic evidence of human immunodeficiency virus exposure
  • Patients with active uncontrolled infection. Patients that are HIV positive or test positive on HBs or HCV antigens.
  • Pregnant or lactating women
  • Serious medical or psychiatric illness which prevent informed consent
  • Patients who are likely to lost to follow up (eg, unwilling or difficult to return, cannot be contacted)
  • Patients with active malignancies

结局指标

主要结局

To investigate the efficacy of alemtuzumab in terms of objective response rate (ORR: complete remission [CR], partial remission [PR]), progression free survival (PFS), and relapse rate in patients with autoimmune cytopenias

次要结局

  • To determine the safety profiles of alemtuzumab in patients with autoimmune cytopenias.

研究者

发起方
Phramongkutklao College of Medicine and Hospital
申办方类型
Other

研究点 (2)

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