The purpose of this study is to assess the safety and efficacy of ABT-493/ABT-530 following 12 weeks of treatment in adults with chronic Hepatitis C Virus Infection genotype 1, 2, 4, 5 or 6 infection and compensated cirrhosis.
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Percentage of Participants With Sustained Virologic Response 12 Weeks Post-treatment (SVR12)
Timeframe: 12 weeks after the last actual dose of study drug