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Moderate Sustained Virologic Response Rates With 6-Week Combination Directly Acting Anti–Hepatitis C Virus Therapy in Patients With Advanced Liver Disease
Author(s) -
Sarah Kattakuzhy,
Eleanor Wilson,
Sreetha Sidharthan,
Zayani Sims,
Mary McLaughlin,
Angie Price,
Rachel Silk,
Chloe Gross,
Elizabeth Akoth,
Maryellen McManus,
Benjamin Emmanuel,
Shikha Shrivastava,
Lydia Tang,
Amy Nelson,
Gebeyehu Teferi,
José Chávez,
Brian Lam,
Hongmei Mo,
A. Osinusi,
Michael A. Polis,
Henry Masur,
Anita Kohli,
Shyamasundaran Kottilil
Publication year - 2015
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1093/cid/civ897
Subject(s) - medicine , ledipasvir , sofosbuvir , regimen , hepatitis c virus , hepatitis c , gastroenterology , adverse effect , cirrhosis , liver disease , combination therapy , immunology , ribavirin , virus
Treatment of genotype 1 hepatitis C virus (HCV) infection with combination directly acting antivirals (DAA) for 8-24 weeks is associated with high rates of sustained virologic response (SVR). We previously demonstrated that adding a third DAA to ledipasvir and sofosbuvir (LDV/SOF) can result in high SVR rates in patients without cirrhosis. In this study, we investigated whether a similar regimen would yield equivalent rates of cure in patients with advanced liver fibrosis.

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