EUCTR2007-004270-43-IT进行中（未招募）不适用
INTERNATIONAL COLLABORATIVE TREATMENT PROTOCOL FOR CHILDREN AND ADOLESCENTS WITH ACUTE LYMPHOBLASTIC LEUKEMIA - AIEOP-BFM ALL 2009
IVERSITY HOSPITAL SCHLESWIG-HOLSTEIN CAMPUS KIE0 个研究点目标入组 4,750 人开始时间: 2010年11月2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）
- 发起方
- 入组人数
- 4,750
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
- •- newly diagnosed acute lymphoblastic leukemia - age = 1 year (> 365 days) and < 18 years (up to 17 years and 365 days) - no Ph+ (BCR/ABL or t(9;22)-positive) ALL - no evidence of pregnancy or lactation period - no participation in another clinical study - patient enrolled in participating center - written informed consent
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •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
- •- pre-treatment with cytostatic drugs, - steroid pre-treatment with = 1 mg/kg/d for more than two weeks during the last month before diagnosis, - treatment started according to another protocol, - underlying diseases that prohibit treatment according to the protocol (e.g. severe congenital heart disease, Charcot-Marie Syndrome, Ataxia-teleangectasia…), - ALL diagnosed as second malignancy.
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