作者
Cihan Yurdaydın,Zaigham Abbas,Marı́a Buti,Andreas Erhardt,Rafael Esteban,Ohad Etzion,Edward Gane,Robert G. Gish,Jeffrey S. Glenn,Saeed Hamid,Theo Heller,Christopher Koh,Pietro Lampertico,Yoav Lurie,Michael P. Manns,Raymundo Paraná,Mario Rizzetto,Stephan Urban,Heiner Wedemeyer,A. Wranke,Lourdes Maria Pinheiro Borzacov,Cirley Lobato,Saeed Hamid,Emanoil Ceauşu,George Ν. Dalekos,Adela Turcanu,Grazia Anna Niro,Farheen Lubna,Minaam Abbas,Patrick Ingiliz,Péter Ferenci,Thomas Vanwolleghem,Tonya Hayden,Naranjargal Dashdorj,Adriana Moţoc,Svenja Hardtke
摘要
Chronic hepatitis delta represents the most severe form of chronic viral hepatitis. The current treatment of hepatitis delta virus (HDV) infection consists of the use of interferons and is largely unsatisfactory. Several new compounds are currently in development for the treatment of HDV infection. However, surrogate markers that can be used to develop clinical endpoints in HDV infection are not well defined. In the current manuscript, we aimed to evaluate the existing data on treatment of HDV infection and to suggest treatment goals (possible “trial endpoints”) that could be used across different clinical trials.