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临床试验/EUCTR2012-002232-85-IT
EUCTR2012-002232-85-IT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., a subsidiary of Merck & Co., Inc.0 个研究点目标入组 3,250 人开始时间: 2012年10月19日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
3,250

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: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 10
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • 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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