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临床试验/EUCTR2005-001294-99-IT
EUCTR2005-001294-99-IT进行中(未招募)不适用

A randomized two-by-two, multicenter, open-label phase III study of BMS-354825 administered orally at a dose of 50 mg or 70 mg twice daily or 100 mg or 140 mg once daily in subjects with chronic phase Philadelphia chromosome or BCR-ABL positive chronic myelogenous leukemia who are resistant or intolerant to imatinib mesylate (Gleevec). Revised protocol 06 incorporating administrative letters 01, 02, 03, 04 and 05 and amendments 01, 02, 03, 04 and 05 (v1.0 dated 14 Sep 2010).

Bristol-Myers Squibb International Corporation0 个研究点目标入组 400 人开始时间: 2005年8月11日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
400

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

  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • 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

  • 未提供

研究者

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