跳至主要内容
临床试验/NCT02556307
NCT02556307已完成不适用

A Study of the Effectiveness of Peginterferon Alfa-2a (Pegasys) and Ribavirin Treatment in Slovenian Hepatitis C (HCV) Patients

Hoffmann-La Roche0 个研究点目标入组 270 人开始时间: 2009年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
270
主要终点
Percentage of Participants Achieving Sustained Virological Response (SVR) According to Genotype and Previous Treatment

研究概览

简要总结

In this Slovenian, multi-center, observational study, the effectiveness of standard of care Peginterferon alfa-2a + ribavirin treatment in adult patients with chronic hepatitis C (CHC) is examined. Patients were treated for 24- or 48-weeks, as prescribed by the treating physician, followed by a 24-week follow-up period.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

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

入选标准

  • Male and female patients >/= 18 years
  • Positive test for HCV
  • Effective contraception as specified by the Peginterferon alfa-2a and/or ribavirin labels

排除标准

  • Concomitant infection with HIV or hepatitis B
  • Participation in a clinical trial within 30 days prior to study start
  • Any contraindications specified in the Peginterferon alfa-2a and ribavirin product labels

研究组 & 干预措施

Peginterferon alfa-2a + Ribavirin

干预措施: Peginterferon alfa-2a (Drug)

Peginterferon alfa-2a + Ribavirin

干预措施: Ribavirin (Drug)

结局指标

主要结局

Percentage of Participants Achieving Sustained Virological Response (SVR) According to Genotype and Previous Treatment

时间窗: 6 months after the last study drug administration (up to 123.6 weeks)

SVR was defined as participants with undetectable Hepatitis C virus (HCV) ribonucleic acid (RNA) at 24 weeks after completion of treatment. Undetectable HCV RNA was defined as a single last HCV RNA less than (\<) 20 international units per milliliter (IU/mL). SVR was evaluated based on HCV genotype (G1, G2, G3 and G4), participant's interleukin 28B genotype (CC, CT and TT), and previous treatment (treatment naive or previous treatment).

次要结局

  • Percentage of Participants With Undetectable HCV RNA(Weeks 4, 12 and at end of treatment (up to 99.6 weeks))
  • HCV RNA Values(Baseline; Weeks 4, 12, end of treatment (up to 99.6 weeks) and 6 months after end of treatment (up to 123.6 weeks))
  • Leukocyte Values(Baseline; Weeks 4, 12, end of treatment (up to 99.6 weeks) and 6 months after end of treatment (up to 123.6 weeks))
  • Hemoglobin Values(Baseline; Weeks 4, 12, end of treatment (up to 99.6 weeks) and 6 months after end of treatment (up to 123.6 weeks))
  • Treatment Duration (in Weeks) With Peginterferon Alfa-2a and Ribavirin(Up to 99.6 Weeks)
  • Thrombocyte Values(Baseline; Weeks 4, 12, end of treatment (up to 99.6 weeks) and 6 months after end of treatment (up to 123.6 weeks))

研究者

申办方类型
Industry
责任方
Sponsor

相似试验