EUCTR2005-002801-22-GB进行中(未招募)1 期
Carboplatin Plus Xeloda Followed By Maintenance Xeloda (CARBOX) - CARBOX
The Royal Marsden NHSF Trust0 个研究点目标入组 20 人开始时间: 2006年5月10日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 20
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
入选标准
- •Recurrent, histologically verified epithelial ovarian carcinoma.
- •Measurable disease as assessed by CT in accordance with RECIST guidelines
- •No more than 2 lines of prior chemotherapy (either as adjuvant or for metastatic disease).
- •There must be a platinum-free interval of at least 6 months between platinum therapy and start of the next chemotherapy.
- •A glomerular filtration rate of greater than or equal to 60ml/minute. This can be measured by an EDTA clearance or 24 hour urine collection.
- •Serum bilirubin<2 x institutional upper limit of normal.
- •Patients should have a projected life expectancy of at least 3 months.
- •ECOG performance status 0, 1 or 2.
- •Patients must not have a history of other malignant diseases other than treated non-melanotic skin cancer or in situ carcinoma of the uterine cervix.
- •Adequate bone marrow function WBC>3x109/l, neutrophils>1.5x109/l, platelets>100x109/l.
- •Written informed consent from the patient.
- •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
- •Any medical or psychiatric condition that impairs the patient’s ability to give informed consent.
- •Uncontrolled angina pectoris, heart failure, or clinically significant uncontrolled cardiac arrhythmias.
- •Significant abnormal ECG or cardiac history having a LVEF of less than the lower limit of normal for institution as determined by MUGA scan or echocardiogram.
- •Any other serious uncontrolled medical conditions
- •Pregnancy or lactation (Any woman of child-bearing potential must have a pregnancy test prior to randomisation and must take adequate precautions to prevent pregnancy during treatment).
- •Inability to complete the quality of life questionnaire
研究者
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