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Clinical Trial Summary

Follow-up for durability of sustained virologic response, changes in liver function and safety in patients with SVR24 in feeder studies


Clinical Trial Description

The purpose of this study is to follow patients from the feeder studies who have achieved SVR24 to assess durability of SVR24, and to assess the changes in liver disease, development of hepatocellular carcinoma and post-treatment safety over time. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT02753699
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date December 2011
Completion date May 2015

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