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Journal of Hepatology
Volume 50, Issue 2
, Pages
402-411
, February 2009
Ribavirin: Current role in the optimal clinical management of chronic hepatitis C
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Increased rates of SVR by prevention of relapse in patients with chronic HCV after the addition of ribavirin to 48 weeks’ treatment with pegylated interferon alfa [12].
Increased rates of SVR by prevention of relapse in patients with chronic HCV after the addition of ribavirin to 48 weeks’ treatment with pegylated interferon alfa [12].
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SVR rates in patients with genotype 1 chronic HCV in pivotal trials of peginterferon alfa plus ribavirin. (a) SVR rates following 48 weeks of peginterferon alfa-2a plus 800
mg/day ribavirin [12] and 48SVR rates in patients with genotype 1 chronic HCV in pivotal trials of peginterferon alfa plus ribavirin. (a) SVR rates following 48 weeks of peginterferon alfa-2a plus 800
mg/day ribavirin [12] and 48 weeks of peginterferon alfa-2a plus 800
mg/day or standard dose ribavirin at 1000/1200
mg/day [13]. (b) SVR rates following 48 weeks of peginterferon alfa-2b plus 800
mg/day ribavirin [11] and 48 weeks of peginterferon alfa-2b plus ribavirin at 800
mg/day or weight-based dosing at 800–1400
mg/day [43]. -
The relationship between ribavirin dose and probability of an SVR in patients with chronic HCV treated with peginterferon alfa-2a plus ribavirin. (a) In genotype 1 patients. (b) In genotype 2/3 patienThe relationship between ribavirin dose and probability of an SVR in patients with chronic HCV treated with peginterferon alfa-2a plus ribavirin. (a) In genotype 1 patients. (b) In genotype 2/3 patients [40].
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The impact of ribavirin dose reductions on relapse rates in patients with genotype 1 chronic HCV treated with peginterferon alfa-2a plus ribavirin [14].The impact of ribavirin dose reductions on relapse rates in patients with genotype 1 chronic HCV treated with peginterferon alfa-2a plus ribavirin [14].
☆ The authors declared that they have a relationship with the manufacturers of ribavirin. They received funding from the manufacturers to carry out research for this manuscript. S.Z. declared that he is on the speakers bureau, does consultancy and clinical investigation for La Roche and Schering Plough. He received support for literature search and editorial assistance from La Roche. D.R.N. declared he has a relationship with the manufacturers of the drugs involved. He did not receive funding from the manufacturers to carry out this study.
PII: S0168-8278(08)00717-4
doi: 10.1016/j.jhep.2008.11.006
© 2008 European Association for the Study of the Liver. Published by Elsevier Inc. All rights reserved.
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Journal of Hepatology
Volume 50, Issue 2
, Pages
402-411
, February 2009
