<p>Forest plot showing the results of the final multivariate logistic regression analyses of factors associated with <b>[A]</b> SVR12 and <b>[B]</b> viral relapse in patients receiving 12 weeks of treatment.</p
Effective antiviral therapy is essential for achieving sustained virological response (SVR) in hepat...
International audienceBackground. Simeprevir is approved with pegylated interferon and ribavirin (PR...
The phase IIb, double-blind, placebo-controlled PILLAR trial investigated the efficacy and safety of...
Background: Shortening duration of peginterferon-based HCV treatment reduces associated burden for p...
Background: Shortening duration of peginterferon-based HCV treatment reduces associated burden for p...
Shortening duration of peginterferon-based HCV treatment reduces associated burden for patients. Pri...
HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 weeks as part o...
Background HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 week...
Background & Aims: Simeprevir is an oral, once-daily inhibitor of hepatitis c virus (HCV) protease N...
BACKGROUND:HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 week...
Background: HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 wee...
Background & Aims Simeprevir (SMV) is a once-daily (QD), oral hepatitis C virus (HCV) NS3/4A proteas...
Abstract Background This Phase 3, open-label, rollover study (NCT01323244) investigated the efficacy...
BACKGROUND & AIMS: Simeprevir is an oral, once-daily inhibitor of hepatitis c virus (HCV) pro...
Background & AimsSimeprevir is an oral, once-daily inhibitor of hepatitis c virus (HCV) protease NS3...
Effective antiviral therapy is essential for achieving sustained virological response (SVR) in hepat...
International audienceBackground. Simeprevir is approved with pegylated interferon and ribavirin (PR...
The phase IIb, double-blind, placebo-controlled PILLAR trial investigated the efficacy and safety of...
Background: Shortening duration of peginterferon-based HCV treatment reduces associated burden for p...
Background: Shortening duration of peginterferon-based HCV treatment reduces associated burden for p...
Shortening duration of peginterferon-based HCV treatment reduces associated burden for patients. Pri...
HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 weeks as part o...
Background HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 week...
Background & Aims: Simeprevir is an oral, once-daily inhibitor of hepatitis c virus (HCV) protease N...
BACKGROUND:HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 week...
Background: HCV GT4 accounts for up to 20% of HCV infections worldwide. Simeprevir, given for 12 wee...
Background & Aims Simeprevir (SMV) is a once-daily (QD), oral hepatitis C virus (HCV) NS3/4A proteas...
Abstract Background This Phase 3, open-label, rollover study (NCT01323244) investigated the efficacy...
BACKGROUND & AIMS: Simeprevir is an oral, once-daily inhibitor of hepatitis c virus (HCV) pro...
Background & AimsSimeprevir is an oral, once-daily inhibitor of hepatitis c virus (HCV) protease NS3...
Effective antiviral therapy is essential for achieving sustained virological response (SVR) in hepat...
International audienceBackground. Simeprevir is approved with pegylated interferon and ribavirin (PR...
The phase IIb, double-blind, placebo-controlled PILLAR trial investigated the efficacy and safety of...