PMC5411384BACKGROUND: The aim of the study was to determine the efficacy and safety of triple therapy with a first-generation protease inhibitor (PI; boceprevir, telaprevir) plus peginterferon alfa-2a or -2b plus ribavirin, and dual therapy (peginterferon alfa-2a or -2b plus ribavirin) in patients with chronic hepatitis C (CHC) in routine clinical practice. METHODS: PegBase was an international, prospective, observational study in which 4441 patients with CHC were enrolled in 27 countries. This analysis focuses on results in 4100 treatment-naive and previously treated patients treated with PI-based triple therapy or dual therapy, according to the discretion of the investigator and local standards of practice. The primary efficacy outcome wa...
AIM: To evaluate addition of boceprevir to peginterferon/ribavirin (PR) in Russian patients with chr...
AIM: To check the safety and efficacy of boceprevir/ telaprevir with peginterferon/ribavirin for hep...
A randomized, double-blind, multinational, phase 3 study was conducted comparing the efficacy and sa...
The aim of the study was to determine the efficacy and safety of triple therapy with a first-generat...
BACKGROUND: The aim of the study was to determine the efficacy and safety of triple therapy with a f...
Background and aims: Clinical trials of therapy against chronic hepatitis C virus (HCV) infection in...
BACKGROUND AND AIMS: Clinical trials of therapy against chronic hepatitis C virus (HCV) infection in...
Background: Triple therapy with Pegylated-Interferon α (PEG-IFNα)/Ribavirin (RBV) and Boceprevir (...
Clinical trials of therapy against chronic hepatitis C virus (HCV) infection including boceprevir (B...
Introduction Boceprevir was not previously studied with peginterferon alfa-2a/ribavirin in phase II...
International audienceBACKGROUND & AIMS: We investigated the effectiveness of the protease inhibitor...
AIM:To check the safety and efficacy of boceprevir/telaprevir with peginterferon/ribavirin for hepat...
BACKGROUND:A randomized, double-blind, multinational, phase 3 study was conducted comparing the effi...
BackgroundIn 2011, the FDA approved telaprevir (TVR) and boceprevir (BOC) for use with pegylated int...
Background/purpose: The role of directly-acting antivirals (DAA)-containing regimens in the treatmen...
AIM: To evaluate addition of boceprevir to peginterferon/ribavirin (PR) in Russian patients with chr...
AIM: To check the safety and efficacy of boceprevir/ telaprevir with peginterferon/ribavirin for hep...
A randomized, double-blind, multinational, phase 3 study was conducted comparing the efficacy and sa...
The aim of the study was to determine the efficacy and safety of triple therapy with a first-generat...
BACKGROUND: The aim of the study was to determine the efficacy and safety of triple therapy with a f...
Background and aims: Clinical trials of therapy against chronic hepatitis C virus (HCV) infection in...
BACKGROUND AND AIMS: Clinical trials of therapy against chronic hepatitis C virus (HCV) infection in...
Background: Triple therapy with Pegylated-Interferon α (PEG-IFNα)/Ribavirin (RBV) and Boceprevir (...
Clinical trials of therapy against chronic hepatitis C virus (HCV) infection including boceprevir (B...
Introduction Boceprevir was not previously studied with peginterferon alfa-2a/ribavirin in phase II...
International audienceBACKGROUND & AIMS: We investigated the effectiveness of the protease inhibitor...
AIM:To check the safety and efficacy of boceprevir/telaprevir with peginterferon/ribavirin for hepat...
BACKGROUND:A randomized, double-blind, multinational, phase 3 study was conducted comparing the effi...
BackgroundIn 2011, the FDA approved telaprevir (TVR) and boceprevir (BOC) for use with pegylated int...
Background/purpose: The role of directly-acting antivirals (DAA)-containing regimens in the treatmen...
AIM: To evaluate addition of boceprevir to peginterferon/ribavirin (PR) in Russian patients with chr...
AIM: To check the safety and efficacy of boceprevir/ telaprevir with peginterferon/ribavirin for hep...
A randomized, double-blind, multinational, phase 3 study was conducted comparing the efficacy and sa...