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临床试验/EUCTR2012-002232-85-HU
EUCTR2012-002232-85-HU进行中(未招募)1 期

A Long-Term Follow-up Study to Evaluate the Durability of Virologic Response and/or Viral Resistance Patterns of Subjects With Chronic Hepatitis C Who Have Been Previously Treated with MK-5172 in a Prior Clinical Trial

Merck Sharp & Dohme Corp.0 个研究点开始时间: 2014年2月6日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. HCV infected subjects who previously participated in an MK-5172 protocol and received at least one dose of MK-5172.
  • 2. Subject must enroll (Visit 1) within one year of the treatment portion of their previous MK-5172 protocol.
  • 3. Subject must be = 18 years of age and willing to give written informed consent.
  • 4. Subjects, who have consented for the trial, may also provide consent for Future Biomedical Research. However, the subject may participate in the main trial without participating in Future Biomedical Research.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 219
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 13

排除标准

  • 1. In the opinion of the investigator, if a subject is mentally or legally incapacitated at entry, the subject may be excluded.

研究者

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