EUCTR2008-005295-27-GB进行中（未招募）不适用
A NOVEL HYBRID PROTOCOL FOR RELAPSED GERM CELL TUMOURSWITH POOR PROGNOSIS - GAMIO
Barts and The London NHS Trust0 个研究点目标入组 47 人开始时间: 2009年4月16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
- 47
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
- Male
入选标准
- •1.Germ Cell Tumour (GCT)
- •2.Relapsed or progression on or following platinum-based chemotherapy (rising tumour markers or progressive disease on CT)
- •3.Neutrophil count > 1.0 x109/l
- •4.Platelets > 70 x109/l
- •5.Haemoglobin > 100g/l (may be transfused)
- •6.Calculated Creatinine clearance > 60mls/min or EDTA clearance of > 40ml/min
- •7.Age 16-65 years (Patient under 35 must have a raised LDH at relapse)
- •8.ECOG Performance status 0-3
- •9. FDG-PET CT scans prior to chemotherapy (within 14 days of study entry).
- •Are the trial subjects under 18? yes
- •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
- •1 Other malignancy except basal cell carcinoma
- •2Significant co-morbidity likely to make delivery of this treatment unsafe
- •3Currently enrolled in any other investigational drug study
- •4Unable or unwilling to give written informed consent
研究者
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