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Integrated Efficacy and Safety Analysis of GT1-6 Treatment-Naïve, Non-Cirrhotic
and Compensated Cirrhotic Patients Who Received 8 Weeks of Glecaprevir/Pibrentasvir
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EASL 2020 Aug 27-29 virtual
Reported by Jules Levin
Eli Zuckerman1, Julio Gutierrez2, Douglas E Dylla3, Victor de Ledinghen4, Andrew Muir5, Michael Gschwantler6, Massimo Puoti7, Jihad Slim8, Frederik Nevens9, Linda M Fredrick3, Ana Gabriela Pires dos Santos3, Lino Rodrigues Jr3, John Dillon101Liver Unit, Carmel Medical Center, Faculty of Medicine, Technion Institute, Haifa, Israel; 2St. Vincent Medical Center, Los Angeles, California, United States; 3AbbVie Inc., North Chicago, Illinois, United States; 4Centre d'Investigation de la Fibrose Hepatique, Bordeaux University Hospital, Pessac, France; INSERM U1053, Bordeaux University, Bordeaux, France; 5Duke Clinical Research Institute, Durham, North Carolina, United States; 6Department of Internal Medicine IV, Wilhelminenspital, Vienna, Austria; Sigmund Freud University, Vienna, Austria; 7Niguarda ca Grande Hospital, Milan, Italy; 8Infectious Disease Division, Department of Internal Medicine, St. Michael's Medical Center, Newark, New Jersey, United States; 9Department of Gastroenterology and Hepatology, University Hospitals Leuven, KU Leuven, Belgium; 10Division of Molecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, United Kingdom
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