Background: Entecavir (ETV) 0.5 mg was superior to lamivu-dine 100 mg for virologic, histologic and biochemical end-points at Week 48 in nucleoside-naïve HBeAg(-) chronichepatitis B (CHB) patients (ETV-027). Patients that met protocol-defined endpoints were taken off therapy after 52 weeks. Sub-jects who relapsed within 6 months could re-enroll in ETV-901.We report results of ETV re-treatment through 3 years in studyETV-901. Methods: The HBeAg(-) ETV re-treatment cohort con-sists of patients who enrolled into ETV-901 with a treatmentgap of at least 60 days between studies and received re-treat-ment with 1 mg of ETV. The proportions of patients with HBVDNA <300 copies/mL by PCR assay and ALT normalizationwere evaluated among patients with av...
Aim of the study was to assess the 3-year effectiveness and safety of Entecavir (ETV) in NUC-na\uefv...
BACKGROUND: The aim of this study was to determine the efficacy of entecavir followed by lamivudine ...
Background: Recent data suggest that oral third-generation nucleos(t)ide analogs (NA) monoprophylaxi...
Background/Aims: To evaluate the off-treatment durability of response in HBeAg-negative chronic hepa...
Sustained virologic suppression is a primary goal of therapy for chronic hepatitis B (CHB). In study...
Sustained virologic suppression is a primary goal of therapy for chronic hepatitis B (CHB). In study...
Background: The primary aims of antiviral therapy for the treatment of chronic hepatitis B (CHB) ar...
Background: Entecavir (ETV) 0.5 mg resulted in improved liverhistology and was superior to lamivudin...
Background and Aims: Whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) differentially ...
Background and aims. Entecavir (ETV) is effective and safe in patients with chronic hepatitis B in t...
BACKGROUND & AIMS: Entecavir demonstrated superior benefit to lamivudine at 48 weeks in nucleoside-n...
Background: The primary aims of antiviral therapy for the treatment of chronic hepatitis B (CHB) ar...
BACKGROUND AND OBJECTIVE: The off-treatment durability of nucleos(t)ide analogue therapy in Asian he...
Background/Aims: We investigated the efficacy of entecavir in lamivudine-experienced and -naive pati...
Aim: The efficacy of entecavir (ETV) in treatment-experienced chronic hepatitis B (CHB) patients rem...
Aim of the study was to assess the 3-year effectiveness and safety of Entecavir (ETV) in NUC-na\uefv...
BACKGROUND: The aim of this study was to determine the efficacy of entecavir followed by lamivudine ...
Background: Recent data suggest that oral third-generation nucleos(t)ide analogs (NA) monoprophylaxi...
Background/Aims: To evaluate the off-treatment durability of response in HBeAg-negative chronic hepa...
Sustained virologic suppression is a primary goal of therapy for chronic hepatitis B (CHB). In study...
Sustained virologic suppression is a primary goal of therapy for chronic hepatitis B (CHB). In study...
Background: The primary aims of antiviral therapy for the treatment of chronic hepatitis B (CHB) ar...
Background: Entecavir (ETV) 0.5 mg resulted in improved liverhistology and was superior to lamivudin...
Background and Aims: Whether entecavir (ETV) and tenofovir disoproxil fumarate (TDF) differentially ...
Background and aims. Entecavir (ETV) is effective and safe in patients with chronic hepatitis B in t...
BACKGROUND & AIMS: Entecavir demonstrated superior benefit to lamivudine at 48 weeks in nucleoside-n...
Background: The primary aims of antiviral therapy for the treatment of chronic hepatitis B (CHB) ar...
BACKGROUND AND OBJECTIVE: The off-treatment durability of nucleos(t)ide analogue therapy in Asian he...
Background/Aims: We investigated the efficacy of entecavir in lamivudine-experienced and -naive pati...
Aim: The efficacy of entecavir (ETV) in treatment-experienced chronic hepatitis B (CHB) patients rem...
Aim of the study was to assess the 3-year effectiveness and safety of Entecavir (ETV) in NUC-na\uefv...
BACKGROUND: The aim of this study was to determine the efficacy of entecavir followed by lamivudine ...
Background: Recent data suggest that oral third-generation nucleos(t)ide analogs (NA) monoprophylaxi...