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Clinical Trial Summary

To evaluate Sustained Virologic Response at post treatment Week 12 (SVR12)following treatment with Lambda/RBV/DCV in chronic HCV GT-1, -2, -3 or -4 subjects co-infected with HIV-1


Clinical Trial Description

Study Classification: Safety/Efficacy and Pharmacokinetics/dynamics GT=genotype ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01866930
Study type Interventional
Source Bristol-Myers Squibb
Contact
Status Terminated
Phase Phase 3
Start date July 11, 2013
Completion date August 27, 2015

See also
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