Ledipasvir and Sofosbuvir for Previously Treated HCV Genotype 1 Infection
The University of Texas Health Science Center at San Antonio · Hadassah Medical Center · +20 more institutions
Abstract
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.
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.
Citation impact
- FWCI
- 130.01
- Percentile
- 100%
- References
- 10
Authors
25- NHNezam H. AfdhalCorresponding
The University of Texas Health Science Center at San Antonio, Hadassah Medical Center, The University of Texas Medical Branch at Galveston
- KRK. Rajender Reddy
University of Pennsylvania, Philadelphia University
- DRDavid R. Nelson
University of Florida
- ELEric Lawitz
Texas Liver Institute, The University of Texas Health Science Center at San Antonio
- SCStuart C. Gordon
Henry Ford Health System
Topics & keywords
- Ledipasvir
- Medicine
- Sofosbuvir
- Ribavirin
- Internal medicine
- Adverse effect
- Gastroenterology
- Hepatitis C
- Good health and well-being