EUCTR2006-001989-16-AT进行中(未招募)不适用
Phase II study of Oxaliplatin / Irinotecan / Cetuximab as first line therapy in locally advanced or metastatic gastric cancer
AGMT0 个研究点开始时间: 2006年11月13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
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
- •Signed informed consent
- •Histologically proven gastric adenocarcinoma
- •Measurable or evaluable, inoperable locally advanced or metastatic disease
- •No previous palliative chemotherapy and/or immunotherapy
- •Life expectancy of more than 3 months
- •Age above 18 years
- •WHO performance status ? 2 (Appendix 1)
- •Negative pregnancy test (for female patients with reproduction potential and adequate contraception)
- •Hematological status:
- •Leucocytes ? 3 x 109/l
- •Platelets ? 100 x 109/l
- •Renal function:
- •Serum creatinine: ? 1.5 x upper normal limit of the normal range of the laboratory Hepatic function:
- •-Alkaline phosphatase: < 2.5 x upper normal limit of the normal range of the laboratory or < 5 x if hepatic metastases were present
- •-total Bilirubin level ? 1.5 x upper normal limit of the normal range of the laboratory
- •Baseline evaluations performed before treatment start: clinical and blood evaluations no more than 2 weeks prior to planned first course; tumoral assessment (CT scan or MRI, X- ray) no more than 4 weeks prior to planned first course
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years)
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years)
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Women of child bearing potential not using a contraceptive method
- •Pregnant or breast-feeding women
- •Concomitant antitumoral treatment
- •Adjuvant chemotherapy with Oxaliplatin and/or Irinotecan
- •Prior history of chronic enteropathy, chronic diarrhea, unresolved bowel obstruction/subobstruction, or extensive abdominopelvic radiation therapy
- •Participation in another clinical trial with any investigational drug within 30 days prior to inclusion
- •Peripheral neuropathy (NCI CTC ? grade 1)
- •Previous malignancy other than CRC in the last 5 years except basal cell carcinoma of the skin and/or in situ carcinoma of the cervix
- •Legal incapacity or limited legal capacity
- •Other uncontrolled serious non malignant diseases:
- •Uncontrolled congestive heart failure, angina pectoris, hypertension or arrhythmias, hepatic disease, history of significant neurologic or psychiatric disorders, active infection
研究者
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