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临床试验/JPRN-jRCT2080221290
JPRN-jRCT2080221290未知2 期

A randomized phase II trial of TSU-68 in combination with TS-1 and CDDP versus TS-1 and CDDP in patients with advanced gastric cancer

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 92 人开始时间: 2010年11月1日最近更新:
适应症

试验速览

阶段
2 期
入组人数
92

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

  • 1)Histologically or cytologically proven unresectable or recurrent gastric adenocarcinoma.
  • 2)Target lesions confirmed by Imaging-based evaluation such as CT within 28 days before enrollment.
  • 3)No prior treatment (ex. radiation therapy, chemotherapy, hormonal therapy) for gastric cancer.
  • 4)Adequate oral intake.
  • 5)ECOG Performance Status of 0 to 1.

排除标准

  • 1)Contraindication to TS-1 or CDDP.
  • 2)Severe complications.
  • 3)Colon disorder with active inflammation.
  • 4)History of severe thrombosis or embolism.
  • 5)Active double cancer.

研究者

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