跳至主要内容
临床试验/NCT01753557
NCT01753557已完成3 期

A Phase 3 Study of MP-424 in Combination With PEG-IFN Alfa-2a and RBV, in Subjects With Genotype 1 Hepatitis C, Who Are Treatment-Naïve or Relapsed After Previous Treatment

Tanabe Pharma Corporation1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2012年12月1日最近更新:
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
54
试验地点
1
主要终点
Undetectable HCV (Hepatitis C Virus) RNA (Ribonucleic Acid) at 24 Weeks After Completion of Drug Administration (SVR, Sustained Viral Response)

研究概览

简要总结

This study will evaluate the efficacy and safety of MP-424 with PEG-IFN Alfa-2a and RBV in patients with genotype 1 hepatitis C, who are naïve to its treatment or relapsed after previous treatment.

研究设计

研究类型
Interventional
分配方式
Na
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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Genotype 1 CHC
  • treatment-naïve or relapsers (patient who relapsed after previous treatment)
  • Able and willing to follow contraception requirements

排除标准

  • Cirrhosis of the liver or hepatic failure
  • Hepatitis B surface antigen-positive or HIV (Human Immunodeficiency Virus) antibodies-positive
  • History of, or concurrent hepatocellular carcinoma
  • History of, or concurrent depression, schizophrenia, or suicide attempt in the past
  • Pregnant, lactating, or suspected pregnant patients, or male patients whose female partner is pregnant

研究组 & 干预措施

Treatment-Naive

Experimental

干预措施: MP-424 (Drug)

Treatment-Naive

Experimental

干预措施: RBV (Drug)

Treatment-Naive

Experimental

干预措施: PEG-IFN alfa-2a (Drug)

Treatment-Relapsed

Experimental

干预措施: MP-424 (Drug)

Treatment-Relapsed

Experimental

干预措施: RBV (Drug)

Treatment-Relapsed

Experimental

干预措施: PEG-IFN alfa-2a (Drug)

结局指标

主要结局

Undetectable HCV (Hepatitis C Virus) RNA (Ribonucleic Acid) at 24 Weeks After Completion of Drug Administration (SVR, Sustained Viral Response)

时间窗: 48 weeks

次要结局

  • Undetectable HCV RNA at 4 Weeks After Beginning of Drug Administration (RVR, Rapid Viral Response)(4 weeks)
  • Viral Sequencing at the Non-structural 3 Protease Region of HCV Virus(Result of Resistance-associated Variants Analysis)(From baseline to 24 weeks after completion of drug administration)
  • Undetectable HCV RNA at Completion of Drug Administration (ETR, End-of-treatment Response)(24 weeks)
  • Undetectable HCV RNA at 12 Weeks After Completion of Drug Administration(36 weeks)
  • Transition of Serum HCV RNA Levels(baseline,Day2,Day3,1Weeks,2Weeks,3Weeks,4Weeks,End of treatment,Follow-up 12weeks,Follow-up 24weeks)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

Efficacy and Safety of MP-424, Peginterferon Alfa-2a... | 临床试验