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      Combination of Tenofovir Disoproxil Fumarate and Peginterferon α-2a Increases Loss of Hepatitis B Surface Antigen in Patients With Chronic Hepatitis B.

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          Abstract

          Patients chronically infected with the hepatitis B virus rarely achieve loss of serum hepatitis B surface antigen (HBsAg) with the standard of care. We evaluated HBsAg loss in patients receiving the combination of tenofovir disoproxil fumarate (TDF) and peginterferon α-2a (peginterferon) for a finite duration in a randomized trial.

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          Author and article information

          Journal
          Gastroenterology
          Gastroenterology
          Elsevier BV
          1528-0012
          0016-5085
          Jan 2016
          : 150
          : 1
          Affiliations
          [1 ] Service d'Hépatologie, Hôpital Beaujon, University Paris-Diderot, Inserm Centre de Recherche sur l'Inflammation, Clichy, France.
          [2 ] Division of Gastroenterology, Yonsei University College of Medicine, Seoul, South Korea.
          [3 ] Drexel University College of Medicine, Philadelphia, Pennsylvania.
          [4 ] National Institute for Infectious Diseases, "Matei Bals", Bucharest, Romania.
          [5 ] Kyungpook National University Hospital, Daegu, South Korea.
          [6 ] Toronto Liver Center, Toronto, Canada.
          [7 ] Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, Taiwan.
          [8 ] Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
          [9 ] University of Istanbul, Cerrahpasa Medical Faculty, Istanbul, Turkey.
          [10 ] Liver Clinic, Surat, India.
          [11 ] IFI Institute for Interdisciplinary Medicine at the Asklepios Klinik St. George, University of Hamburg, Hamburg, Germany.
          [12 ] Queen Mary University of London, London, United Kingdom.
          [13 ] Nexus Development, Palo Alto, California.
          [14 ] Gilead Sciences Inc, Foster City, California.
          [15 ] Academic Medical Center, Amsterdam, The Netherlands.
          [16 ] University of Toronto, Department of Medicine, Toronto General Hospital, Toronto, Canada.
          [17 ] AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital and University of Sydney, Sydney, Australia.
          [18 ] San Jose Gastroenterology, San Jose, California.
          [19 ] Hepatology Unit, Hospital Universitari Vall d'Hebron and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas del Instituto Carlos III, Barcelona, Spain.
          [20 ] Viral Hepatitis Unit, Department of Clinical and Experimental Medicine, Second University of Naples, Naples, Italy.
          [21 ] The Chinese University of Hong Kong, Alice Ho Miu Ling Nethersole Hospital, Hong Kong.
          [22 ] Athens University Medical School, "Laiko" General Hospital of Athens, Athens, Greece.
          [23 ] Department of Infectious Diseases and Hepatology, Medical University of Bialystok, Bialystok, Poland.
          [24 ] Department of Medicine and Therapeutics and Institute of Digestive Disease, The Chinese University of Hong Kong, Hong Kong. Electronic address: hlychan@cuhk.edu.hk.
          Article
          S0016-5085(15)01429-8
          10.1053/j.gastro.2015.09.043
          26453773
          8bd37722-74a2-4890-b081-d0d6f3a3ddab
          History

          Clinical Trial,HBV,HBeAg Seroconversion,Virologic Response

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