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临床试验/NCT01297270
NCT01297270已完成3 期

A Phase III, Randomized, Double Blind and Placebo Controlled Study of Once Daily BI 201335 120 mg for 24 Weeks and BI 201335 240 mg for 12 Weeks in Combination With Pegylated Interferon Alpha and Ribavirin in Treatment Naive Patients With Genotype 1 Chronic Hepatitis C Infection.

Boehringer Ingelheim106 个研究点 分布在 1 个国家目标入组 658 人开始时间: 2011年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
658
试验地点
106
主要终点
Sustained Virologic Response 12 Weeks Post Treatment (SVR12)

研究概览

简要总结

The objective of this trial is to evaluate the efficacy and safety of two different treatment regimens with BI 201335, both in combination with PegIFN/RBV) as compared to standard of care (SOC) with PegIFN/RBV alone.

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
Double

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

PegIFN/RBV

Active Comparator

48 weeks

干预措施: PegIFN/RBV (Drug)

BI 201335 for 24 weeks

Experimental

BI 201 335 QD dosing in combination with IFN/RBV

干预措施: PegIFN/RBV (Drug)

BI 201335 for 24 weeks

Experimental

BI 201 335 QD dosing in combination with IFN/RBV

干预措施: BI201335 (Drug)

BI201335 for 12 weeks

Experimental

BI 201335 QD doing in combination with PEFG IFN/RBV

干预措施: BI201335 (Drug)

BI201335 for 12 weeks

Experimental

BI 201335 QD doing in combination with PEFG IFN/RBV

干预措施: PegIFN/RBV (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Sustained Virologic Response 12 Weeks Post Treatment (SVR12)

时间窗: 12 weeks post treatment, up to 60 weeks

Percentage of participants with sustained virologic response 12 weeks post treatment (SVR12) defined as plasma Hepatitis C virus Ribonucleic acid (HCV RNA) level\<25 IU/mL (undetected) 12 weeks after the originally planned treatment duration.

次要结局

  • ALT Normalisation: ALT in Normal Range at End of Treatment (EOT) When SVR12=YES(12 weeks post treatment, up to 60 weeks)
  • ALT Normalisation: ALT in Normal Range at End of Treatment (EOT) When SVR12= NO(12 weeks post treatment, up to 60 weeks)
  • ALT Normalisation: ALT in Normal Range 12 Weeks Post-treatment, When SVR12=YES(12 weeks post treatment, up to 60 weeks)
  • ALT Normalisation: ALT in Normal Range 12 Weeks Post-treatment, When SVR12=NO(12 weeks post treatment, up to 60 weeks)
  • Early Treatment Success (ETS)(Week 4 and week 8)
  • Sustained Virologic Response 24 Weeks Post-treatment (SVR24)(24 weeks post treatment, up to 72 weeks)
  • AST Normalisation: AST in Normal Range 12 Weeks Post-treatment, When SVR12=YES(12 weeks post treatment, up to 60 weeks)
  • AST Normalisation: AST in Normal Range at End of Treatment (EOT) When SVR12=NO(12 weeks post treatment, up to 60 weeks)
  • AST Normalisation: AST in Normal Range at End of Treatment (EOT) When SVR12=YES(12 weeks post treatment, up to 60 weeks)
  • AST Normalisation: AST in Normal Range 12 Weeks Post-treatment, When SVR12=NO(12 weeks post treatment, up to 60 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (106)

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