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临床试验/NCT00721916
NCT00721916已完成2 期

Randomized Phase II Study of S-1, Oral Leucovorin, and Oxaliplatin Combination Therapy (SOL) Versus 5-FU, l-LV and Oxaliplatin Combination Therapy (mFOLFOX6) in Patients With Untreated Metastatic Colorectal Cancer

Taiho Pharmaceutical Co., Ltd.1 个研究点 分布在 1 个国家目标入组 107 人开始时间: 2008年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
107
试验地点
1
主要终点
Progression free survival (PFS)

研究概览

简要总结

This is a randomized, multicenter study designed to evaluate the progression free survival of the SOL group (S-1, Leucovorin, and Oxaliplatin) compared with the mFOLFOX6 group (5-FU, l-LV and Oxaliplatin) as first-line treatment of patients with metastatic colorectal cancer.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically proved adenocarcinoma (colorectal cancer).
  • Age: 20 ≤ at enrollment.
  • No prior treatment (ex. radiation therapy, chemotherapy, hormonal therapy) to advanced disease. Patients who received adjuvant chemotherapy more than 180 days before enrollment can be allowed but those who received S-1 or Oxaliplatin containing treatment shall be excluded.
  • At least one measurable lesion by RECIST criteria

排除标准

  • Serious drug hypersensitivity.
  • Prior history of peripheral neuropathy.
  • Diarrhea .
  • Simultaneously active double cancer.

研究组 & 干预措施

1

Experimental

SOL(The combination therapy of S-1, Leucovorin, and Oxaliplatin)

干预措施: SOL(The combination therapy of S-1, Leucovorin, and Oxaliplatin) (Drug)

2

Active Comparator

mFOLFOX6(The combination therapy of 5-FU, l-LV and Oxaliplatin)

干预措施: mFOLFOX6(The combination therapy of 5-FU, l-LV and Oxaliplatin) (Drug)

结局指标

主要结局

Progression free survival (PFS)

时间窗: Until progression

次要结局

  • Safety(During chemotherapy)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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