Sofosbuvir with pegylated interferon alfa-2a and ribavirin for treatment-naive patients with hepatitis C genotype-1 infection (ATOMIC): an open-label, randomised, multicentre phase 2 trial

Summary Background The uridine nucleotide analogue sofosbuvir is a selective inhibitor of hepatitis C virus (HCV) NS5B polymerase. We assessed the safety and efficacy of sofosbuvir in combination with pegylated interferon alfa-2a (peginterferon) and ribavirin in non-cirrhotic treatment-naive, patien...

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Veröffentlicht in:The Lancet (British edition) 2013-06, Vol.381 (9883), p.2100-2107
Hauptverfasser: Kowdley, Kris V, Dr, Lawitz, Eric, MD, Crespo, Israel, MD, Hassanein, Tarek, MD, Davis, Mitchell N, MD, DeMicco, Michael, MD, Bernstein, David E, MD, Afdhal, Nezam, MD, Vierling, John M, MD, Gordon, Stuart C, MD, Anderson, Jane K, PhD, Hyland, Robert H, DPhil, Dvory-Sobol, Hadas, PhD, An, Di, PhD, Hindes, Robert G, MD, Albanis, Efsevia, MD, Symonds, William T, PharmD, Berrey, M Michelle, MD, Nelson, David R, MD, Jacobson, Ira M, MD
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Sprache:eng
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Zusammenfassung:Summary Background The uridine nucleotide analogue sofosbuvir is a selective inhibitor of hepatitis C virus (HCV) NS5B polymerase. We assessed the safety and efficacy of sofosbuvir in combination with pegylated interferon alfa-2a (peginterferon) and ribavirin in non-cirrhotic treatment-naive, patients with HCV. Methods For this open-label, randomised phase 2 trial, we recruited patients from 42 centres in the USA and Puerto Rico between March 23, 2011, and Sept 21, 2011. Patients were eligible for inclusion if they had chronic HCV infection (genotypes 1, 4, 5, or 6), were aged 18 years or older, and had not previously received treatment for HCV infection. Using a computer-generated randomisation sequence, we randomly assigned patients with HCV genotype-1 to one of three cohorts (A, B, and C; in a 1:2:3 ratio), with randomisation stratified by IL28B (CC vs non-CC allele) and HCV RNA (
ISSN:0140-6736
1474-547X
DOI:10.1016/S0140-6736(13)60247-0