Ledipasvir and Sofosbuvir for Previously Treated HCV Genotype 1 Infection

Nezam H. Afdhal(The University of Texas Health Science Center at San Antonio), K. Rajender Reddy(University of Pennsylvania), David R. Nelson(University of Florida), Eric Lawitz(Texas Liver Institute), Stuart C. Gordon(Henry Ford Health System), Eugene R. Schiff(University of Miami), Ronald Nahass, Reem Ghalib(Texas Research Institute), Norman Gitlin(Atlanta Gastroenterology Associates), Robert Herring(Quality Research), Jacob Lalezari(Quest Clinical Research (United States)), Ziad Younes(Gastro One (United States)), Paul J. Pockros(Scripps Clinic), Adrian M. Di Bisceglie, Sanjeev Arora(University of New Mexico), G. Mani Subramanian(Gilead Sciences (United States)), Yanni Zhu(Gilead Sciences (United States)), Hadas Dvory‐Sobol(Gilead Sciences (United States)), Jenny C. Yang(Gilead Sciences (United States)), Phillip S. Pang(Gilead Sciences (United States)), William T. Symonds(Gilead Sciences (United States)), John G. McHutchison(Gilead Sciences (United States)), Andrew J. Muir(Duke Medical Center), Mark Sulkowski(Johns Hopkins Bayview Medical Center), Paul Y. Kwo(Indiana University – Purdue University Indianapolis)
New England Journal of Medicine
April 12, 2014
Cited by 1,306

Abstract

BACKGROUND: Effective treatment for hepatitis C virus (HCV) genotype 1 infection in patients who have not had a sustained virologic response to prior interferon-based therapy represents an unmet medical need. METHODS: We conducted a phase 3, randomized, open-label study involving patients infected with HCV genotype 1 who had not had a sustained virologic response after treatment with peginterferon and ribavirin, with or without a protease inhibitor. Patients were randomly assigned to receive the NS5A inhibitor ledipasvir and the nucleotide polymerase inhibitor sofosbuvir in a once-daily, fixed-dose combination tablet for 12 weeks, ledipasvir-sofosbuvir plus ribavirin for 12 weeks, ledipasvir-sofosbuvir for 24 weeks, or ledipasvir-sofosbuvir plus ribavirin for 24 weeks. The primary end point was a sustained virologic response at 12 weeks after the end of therapy. RESULTS: Among the 440 patients who underwent randomization and were treated, 20% had cirrhosis and 79% had HCV genotype 1a infection. The rates of sustained virologic response were high in all treatment groups: 94% (95% confidence interval [CI], 87 to 97) in the group that received 12 weeks of ledipasvir-sofosbuvir; 96% (95% CI, 91 to 99) in the group that received 12 weeks of ledipasvir-sofosbuvir and ribavirin; 99% (95% CI, 95 to 100) in the group that received 24 weeks of ledipasvir-sofosbuvir; and 99% (95% CI, 95 to 100) in the group that received 24 weeks of ledipasvir-sofosbuvir and ribavirin. No patient discontinued treatment owing to an adverse event. The most common adverse events were fatigue, headache, and nausea. CONCLUSIONS: Treatment with a once-daily, single-tablet regimen of ledipasvir and sofosbuvir resulted in high rates of sustained virologic response among patients with HCV genotype 1 infection who had not had a sustained virologic response to prior interferon-based treatment. (Funded by Gilead Sciences; ION-2 ClinicalTrials.gov number, NCT01768286.).


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