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临床试验/JPRN-jRCT2080221515
JPRN-jRCT2080221515未知2 期

A Randomized Phase II Study of S-1 plus Leucovorin versus S-1 alone in Patients with Gemcitabine-Refractory Advanced Pancreatic Cancer.

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 140 人开始时间: 2011年7月15日最近更新:
适应症

试验速览

阶段
2 期
入组人数
140

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 <= 79age old(—)
性别
All

入选标准

  • Patients must be diagnosed as invasive pancreatic ductal carcinoma
  • - Patients with gemcitabine-refractory
  • - Age: 20 years to 79 years
  • - Eastern Cooperetive Oncology Group (ECOG) performance status (PS) of 0 or 1
  • - Sufficient oral intake
  • - Written informed consent

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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