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临床试验/NCT00245414
NCT00245414已完成4 期

Post-marketing Clinical Trial of Pegasys® 180μg for Subcutaneous Injection in Patients With Chronic Hepatitis C. General Clinical Study in Interferon (IFN)-Treated and IFN-untreated Chronic Hepatitis C Patients, Except for Those Infected With High Viral Load of Genotype 1b

Chugai Pharmaceutical6 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2005年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
108
试验地点
6
主要终点
Sustained viral response as undetectable level of HCV-RNA

研究概览

简要总结

The purpose of this study is to investigate the efficacy and safety of Pegasys® 180μg for subcutaneous (s.c.) injection in interferon (IFN)-treated or IFN-untreated chronic hepatitis C patients except for those infected with genotype 1b of hepatitis C virus (HCV) and a high viral load (≥ 100 KIU/mL).

In addition, this study will explore the efficacy and safety of Pegasys® 180μg for s.c. injection given at 2 different periods between 24 and 48 weeks in IFN-untreated chronic hepatitis C patients.

研究设计

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

入排标准

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

入选标准

  • Quantitative serum HCV-RNA is positive except for high viral load of genotype 1b (≥ 100 KIU/mL)
  • Observation of serum ALT elevation above upper limit of normal
  • Chronic hepatitis is evaluated as the negative result (< 0) calculated by the method of "formula for discrimination between chronic hepatitis and liver cirrhosis."

排除标准

  • Observation of white blood cells ≦ 3000/mm3; neutrophils ≦ 1500/mm3; platelets ≦ 90,000/mm3; or hemoglobin ≦ 10 g/dL.
  • Observation of the following situations and disease: severe renal disease, hepatitis B co-infection, de-compensated liver disease, liver cirrhosis, hepatocellular carcinoma, poorly controlled psychiatric disease, seizure disorders, immunologically mediated disease, severe cardiac disease, poorly uncontrolled hypertension, poorly controlled diabetes, chronic pulmonary disease, retinopathy, malignant tumor, and organ transplant

研究组 & 干预措施

1

Experimental

Interferon (IFN)-Treated

干预措施: Pegasys® (Drug)

2

Experimental

Interferon (IFN)-Untreated and Quantitative serum HCV-RNA is positive at week 1

干预措施: Pegasys® (Drug)

3

Experimental

Interferon (IFN)-Untreated and Quantitative serum HCV-RNA is negative at week 1

干预措施: Pegasys® (Drug)

4

Experimental

Interferon (IFN)-Untreated and Quantitative serum HCV-RNA is negative at week 1

干预措施: Pegasys® (Drug)

结局指标

主要结局

Sustained viral response as undetectable level of HCV-RNA

时间窗: week 24 from the end of treatment

次要结局

  • Biochemical response as normal level of ALT(week 24 from the end of treatment)
  • Viral response as undetectable level of HCV-RNA(at the end of treatment)

研究者

申办方类型
Industry

研究点 (6)

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