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Mensa3 AASLD: Efficacy and Safety of Glecaprevir/Pibrentasvir for 8 or 12 Weeks in Treatment-nave Patients with Chronic HCV Genotype 3: An Integrated Phase 2/3 Analysis - (10/23/17) IAS: Glecaprevir/Pibrentasvir Fixed-Dose Combination for 8 or 12 Weeks in Patients Co-Infected With HCV and HIV-1: A Sub-Analysis of the Phase 3 ENDURANCE-1 Study - (07/24/17) IAS: Efficacy and Safety of Glecaprevir/Pibrentasvir in Patients Co-infected with Hepatitis C Virus and Human Immunodeficiency Virus-1: The EXPEDITION-2 Study - (07/24/17) IAS: Maviret /G-P in HIV+ Coinfected / ART DDIs - (09/12/17) EASL: New HCV Drugs at EASL 2017 - (05/09/17) AASLD: Safety and Efficacy of Glecaprevir / Pibrentasvir in Patients with Chronic Hepatitis C Genotypes 1 - 6 and Recent Drug Use - (11/27/17) AASLD: Safety and Efficacy of Glecaprevir/Pibrentasvir in Patients Aged 65 Years or Older With Chronic Hepatitis C: A Pooled Analysis of Phase 2 and 3 Clinical Trials - (10/29/17) Abstract This study assessed the efficacy and safety of ribavirin-free coformulated glecaprevir/pibrentasvir (G/P) in patients with hepatitis C virus genotype 3 infection with prior treatment experience and/or compensated cirrhosis, a patient population with limited treatment options

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