Your browser doesn't support javascript.
loading
Use of Current and New Endpoints in the Evaluation of Experimental Hepatitis B Therapeutics.
Block, Timothy M; Locarnini, Stephen; McMahon, Brian J; Rehermann, Barbara; Peters, Marion G.
Affiliation
  • Block TM; Hepatitis B Foundation and Baruch S. Blumberg Institute, Doylestown, Pennsylvania, USA.
  • Locarnini S; Victorian Infectious Diseases Reference Laboratory, Doherty Institute, Melbourne, Australia.
  • McMahon BJ; Alaska Native Health Center, Anchorage, USA.
  • Rehermann B; Immunology Section, Liver Diseases Branch, National Institutes of Health, Bethesda, Maryland, USA.
  • Peters MG; Department of Medicine, University of California, San Francisco, USA.
Clin Infect Dis ; 64(9): 1283-1288, 2017 05 01.
Article in En | MEDLINE | ID: mdl-28200098
ABSTRACT
New hepatitis B virus (HBV) therapies are expected to have breakthrough benefit for patients. HBV functional cure is sustained hepatitis B surface antigen loss and anti-HBs gain, with normalization of serum aminotransferases off therapy. Virologic or complete cure additionally includes loss of HBV covalently closed circular DNA. Currently available endpoints of therapy are inadequate to evaluate the efficacy of many of the new therapeutics. Therefore, either new ways of using the existing virologic endpoints and laboratory values or entirely new biomarkers are needed. In this review, we discuss the currently used endpoints, potential new endpoints, as well as what new markers are needed to assess the ability of HBV therapeutics to achieve functional and virologic cure in various phases of HBV infection. In addition, we discuss how patient selection from differing phases of HBV impacts the choice of HBV drug(s) needed to achieve cure.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Hepatitis B, Chronic / Endpoint Determination Limits: Humans Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2017 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers / Hepatitis B, Chronic / Endpoint Determination Limits: Humans Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2017 Type: Article Affiliation country: United States