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临床试验/NCT00048724
NCT00048724已完成3 期

PEG-Intron as Maintenance Therapy vs. an Untreated Control Group in Adult Subjects With Compensated Cirrhosis (METAVIR F4), Secondary to Chronic Hepatitis C, Who Have Failed to Respond to Therapy With Any Alpha Interferon Plus Ribavirin

Merck Sharp & Dohme LLC0 个研究点目标入组 631 人开始时间: 2002年6月最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
631
主要终点
Time to Observation of the First Clinical Event Experienced by a Subject

研究概览

简要总结

The objective of the study is to evaluate the safety and efficacy of PEG-Intron vs. no treatment for the prevention of disease progression in adult subjects with compensated cirrhosis secondary to chronic hepatitis C, who failed to respond to therapy with an a interferon plus ribavirin.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age at entry 18-65 years;
  • Non-responders to previous treatment (minimum of 3 months) with an alpha interferon plus ribavirin;
  • Liver biopsy demonstrating cirrhosis

排除标准

  • Any other cause for liver disease other than chronic hepatitis C;
  • History or presence of complications of cirrhosis;
  • Alcohol or illicit drug abuse or treatment with methadone within the past 2 years;
  • Diseases or conditions that could interfere with participation in the study

结局指标

主要结局

Time to Observation of the First Clinical Event Experienced by a Subject

时间窗: Up to 60 months of treatment or observation, or when 98 subjects experience at least one clinical event

Clinical events are liver decompensation \[variceal bleeding, development of Child-Pugh Class C, hepatic encephalopathy ≥Grade 2, ascites\], hepatic carcinoma, death, and/or liver transplantation

次要结局

  • Time to Observation of the Disease Progression Experienced by a Subject(Up to 60 months of treatment or observation, or when 98 subjects experience at least one clinical event)

研究者

申办方类型
Industry
责任方
Sponsor

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