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3-Year Observational Virology Follow-up Study in Subjects Who Participated in Studies of Idenix Anti-HCV, Direct Acting Antivirals

Hepatitis C Clinical Trial

Official title:
3-Year, Observational Study to Evaluate the Durability of Sustained Viral Response and the Kinetics of Antiviral-Resistant HCV in Subjects Who Participated in Studies of Idenix Anti-HCV, Direct Acting Antivirals

Clinical Trial Summary

All subjects in this study have previously been in an Idenix HCV study and received study drug for 3 consecutive days. Subjects who had received placebo in a previous Idenix study will not be enrolled in this study.

In this study, researchers will try to find answers to these questions:

- How much (if any) hepatitis C virus is in your blood after stopping your Idenix study drug?

- Is your hepatitis C virus possibly resistant to treatment with the Idenix study drug or similar drugs?

Clinical Trial Description

The data obtained from this study will be used to further understand the long-term efficacy of Idenix DAAs used to treat HCV infection and to further understand HCV resistance to Idenix DAAs. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01721265
Study type Observational
Source Merck Sharp & Dohme Corp.
Contact
Status Terminated
Phase N/A
Start date October 2012
Completion date March 2015
View Details
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