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临床试验/EUCTR2007-002143-25-GB
EUCTR2007-002143-25-GB进行中(未招募)1 期

A Phase 1/2a Study Evaluating the Safety, Pharmacokinetics, and Efficacy of ABT-263 in Subjects with Relapsed or Refractory Chronic Lymphocytic Leukemia.

AbbVie Deutschland GmbH & Co. KG0 个研究点目标入组 72 人开始时间: 2008年6月27日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
72

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Chronic or relapsed Chronic Lymphocytic Leukemia and require treatment in the opinion of the investigator.
  • 2. Eastern Cooperative Oncology Group (ECOG) performance score of = 1.
  • 3. Adequate bone marrow independent of growth factor support, renal and hepatic function per defined laboratory criteria.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Has a history or is significantly suspicious for cancer related Central Nervous System (CNS) disease.
  • 2. Receipt of allogenic or autologous stem cell transplant.
  • 3. Recent history (within 1 year of first dose) of underlying, predisposing condition of bleeding or currently
  • exhibit signs of bleeding.
  • 4. Active peptic ulcer disease or other potentially hemorrhagic esophagitis/gastritis.
  • 5. Active immune thrombocytopenic purpura or history of being refractory to platelet transfusions (within 1 year
  • of first dose).

研究者

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