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临床试验/JPRN-jRCT2080221595
JPRN-jRCT2080221595未知2 期

A Randomized Phase II study of S-1 and LV versus S-1, LV and L-OHP versus S-1 and CDDP in Patients with Advanced Gastric Cancer

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 144 人开始时间: 2011年9月26日最近更新:
适应症

试验速览

阶段
2 期
入组人数
144

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • Patients must be diagnosed as advanced gastric cancer
  • - Age: 20 years or order
  • - Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1
  • - Sufficient oral intake
  • - Written informed consent
  • - At least one measurable lesion by RECIST criteria

排除标准

  • - Diarrhea
  • - History or presence of severe pulmonary disease
  • - History or presence of severe heart disease
  • - Uncontrolled or severe diabetes
  • - Severe complications(e.g., severe enteritis, severe stomatitis, gastrointestinal ulcer)

研究者

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