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临床试验/JPRN-jRCT2080221054
JPRN-jRCT2080221054未知2 期

A Phase II study of TSU-68 in patient with hepatocellular carcinoma who are treated by transcatheter arterial chemoembolization (TACE)

Taiho Pharmaceutical Co., Ltd.0 个研究点目标入组 100 人开始时间: 2010年4月1日最近更新:
适应症

试验速览

阶段
2 期
入组人数
100

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)20 years or older.
  • 2)Histopathologically confirmed HCC or diagnosed as HCC by the CT imaging.
  • 3)Not indicated to treatment with curative surgery or percutaneous ablation(such as RFA, PEIT or PMCT).
  • 4)Adequate oral intake.
  • 5)Life expectancy of at least 3 months.
  • 6)P.S.:0-2

排除标准

  • 1)Patient has ascites, pleural effusions or pericardial fluid requiring drainage .
  • 2)Patient has clinical symptoms of hepatic encephalopathy.
  • 3)Patient has active or uncontrolled clinically serious infection excluding
  • chronic hepatitis .
  • 4)Patient has active double cancer.
  • 5)Have participated in other clinical trials within 4 weeks prior to registration.

研究者

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