JPRN-UMIN000006952已完成3 期
A randomised comparison of safety and efficacy of triple therapy for 12 weeks, followed by 12 or 36 additional weeks of peginterferon alfa 2b and ribavirin in HCV patients - Study of 12 or 36 additional weeks of peginterferon alfa 2b and ribavirin
Hiroshima liver study group0 个研究点目标入组 230 人开始时间: 2011年12月26日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 230
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 70years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1)Transient response to prior treatment 2)Patients receiving shosaiko-to 3)Autoimmune hepatitis 4)History of hypersensitivity to PEG-IFN alpha-2b and telaprevir 5)History of hypersensitivity to biological products such as vaccine 6)Decompenstated liver cirrhosis 7)HCC, malignat tumor 8)With or with a history of severe psychosis such as severe depression, suicidal ideation or attempt, etc. 9)Pregnant or lactating women and women who may be pregnant 10)Judged by investigator not to be appropriate for inclusion in this study
研究者
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