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临床试验/EUCTR2006-006852-37-FR
EUCTR2006-006852-37-FR进行中(未招募)不适用

A phase III randomized, double-blind study of induction(daunorubicin/cytarabine) and consolidation (high dose cytarabine) chemotherapy + midostaurin (PKC412) (IND # 101261) or placebo in newly diagnosed patients < 60 years of age with FLT3 mutated acute myeloid leukemia (AML) - CALGB10603/PKC412A2301

ovartis Pharma Services AG0 个研究点目标入组 550 人开始时间: 2008年11月14日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
550

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

  • - Unequivocal diagnosis of AML (> 20% blasts in the bone marrow based on the
  • WHO classification, excluding M3 (acute promyelocytic leukemia)
  • - Documented FLT3 mutation
  • - Age =18 and < 60 years
  • - No prior chemotherapy for leukemia or myelodysplasia with few exception listed
  • (see protocol page 7)
  • - Bilirubin < 2.5 upper limit of normal
  • - Non pregnant and non-nursing
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Patients who have developed therapy related AML after prior RT or chemotherapy
  • for another disorder or cancer
  • - Patients with symptomatic congestive heart failure

研究者

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A phase III randomized, double-blind study of... | 临床试验