JPRN-UMIN000001233已完成2 期
Phase II clinical trial of the first-line Stop-and-Go modified FOLFOX6 and bevacizmab for patients with unresectable/recurrent colorectal cancer - Phase II clinical trial of the first-line Stop-and-Go modified FOLFOX6 and bevacizmab for patients with unresectable/recurrent colorectal cancer
Mlnlstry of health, Labour and Welfare0 个研究点目标入组 50 人开始时间: 2008年7月7日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 75years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)active other malignancies 2)history of the severe drug hypersensitivity 3)clinically significant infectious disease(body temperature less than 38.0 degrees) 4)severe complications (ileus, bowel obstruction, interstitial lung disease, pulmonary fibrosis, uncontrolled diabetes mellitus, heart failure, renal failure, hepatic failure and so on) 5)uncontrollable hypertension 6)urinary protein (more than 1+) 7)Patients who have abnormal findings on ECG and need any treatment (within 2 weeks before the registration.) 8)Moderate/severe pleural effusion or ascites 9)Symptomatic brain metastasis 10)Any significant bleedings 11)Evidence of bleeding diathesis 12)History of thoromboembolitic disease 13)Uncontrolled watery diarrhea. Watery colostomy output without trouble with patient's daily living is allowed. 14)Surgical procedure within 4 weeks before registration (the implanted central venous port is allowed.) 15)Patient who underwents the implantation of the central venous port within a day prior to start of study drugs. 16)Pregnant or lactating women, women who are capable of pregnancy or intend to get pregnant, men who don't intend to have protected intercourse. 17)Any other cases who are regarded as Inadequate for study enrollment by the attending doctors.
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