OBJECTIVE: To evaluate the safety and efficacy of daclatasvir, an HCV NS5A inhibitor with pangenotypic activity, administered with peginterferon-alfa-2a/ribavirin. DESIGN: In this Phase 2b double-blind, placebo-controlled study, treatment-naive adults with HCV genotype 1 (N=365) or 4 (N=30) infection were randomly assigned (2:2:1) to daclatasvir 20 mg or 60 mg, or placebo once daily plus weekly peginterferon-alfa-2a and twice-daily ribavirin. Daclatasvir recipients achieving protocol-defined response (PDR; HCV-RNA
Autori interni: | |
Autori: | Hézode, C; Hirschfield, Gm; Ghesquiere, W; Sievert, W; Rodriguez Torres, M; Shafran, Sd; Thuluvath, Pj; Tatum, Ha; Waked, I; Esmat, G; Lawitz, Ej; Rustgi, Vk; Pol, S; Weis, N; Pockros, Pj; Bourlière, M; Serfaty, L; Vierling, Jm; Fried, Mw; Weiland, O; Brunetto, MAURIZIA ROSSANA; Everson, Gt; Zeuzem, S; Kwo, Py; Sulkowski, M; Bräu, N; Hernandez, D; Mcphee, F; Wind Rotolo, M; Liu, Z; Noviello, S; Hughes, Ea; Yin, Pd; Schnittman, S. |
Titolo: | Daclatasvir plus peginterferon alfa and ribavirin for treatment-naive chronic hepatitis C genotype 1 or 4 infection: a randomised study |
Anno del prodotto: | 2015 |
Abstract: | OBJECTIVE: To evaluate the safety and efficacy of daclatasvir, an HCV NS5A inhibitor with pangenotypic activity, administered with peginterferon-alfa-2a/ribavirin. DESIGN: In this Phase 2b double-blind, placebo-controlled study, treatment-naive adults with HCV genotype 1 (N=365) or 4 (N=30) infection were randomly assigned (2:2:1) to daclatasvir 20 mg or 60 mg, or placebo once daily plus weekly peginterferon-alfa-2a and twice-daily ribavirin. Daclatasvir recipients achieving protocol-defined response (PDR; HCV-RNA |
Digital Object Identifier (DOI): | 10.1136/gutjnl-2014-307498 |
Appare nelle tipologie: | 1.1 Articolo in rivista |
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