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临床试验/JPRN-UMIN000003541
JPRN-UMIN000003541已完成1 期

A phase 1 study of combination chemotherapy for hepatocellular carcinoma using Miripla® (SM11355) and IA-call® (DDP-H) - A combination chemotherapy of SM11355 and DDP-H for HCC (Phase 1)

iigata Hepatocellular Carcinoma Therapy Study Group0 个研究点目标入组 18 人开始时间: 2010年5月1日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
18

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
20years-old 至 79years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Pleural effusion and/or ascites refractory to treatments. 2) Comorbidity: Active infectious diseases except for hepatitis. Active bleeding from GI tract. Active concomitant cancer with invasive nature. Severe mental disorder or hepatic encephalopathy. 3) A history of severe allergic reaction against iodine contrast medium and/or platinum agents. 4) A pregnant or lactating female or female of childbearing age unless using effective contraception. 5) Ongoing interferon therapy. 6) Difficulties of oral intake. 7) Other serious conditions judged to be inadequate by a responsible doctor.

研究者

发起方
iigata Hepatocellular Carcinoma Therapy Study Group

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