374
Participants
Start Date
September 23, 2019
Primary Completion Date
June 30, 2025
Study Completion Date
June 30, 2025
Sofosbuvir/velpatasvir (Epclusa®)
The protocol is intended to follow best practices/standard of care for the treatment of HCV, with additional allowances for the investigators to apply rigorous scientific practices for the research aspects of the study. While the treatment of HCV is fairly straightforward, less is known about treating active drug users and RNA-positive individuals in rural areas. We propose eight visits, including intake, four treatment-related visits, and three visits to determine re-infection (6- and 12-months post-SVR). Because determination of medication adherence and long-term reinfection rates are not part of standard clinical practice, the rural protocol developed at the conclusion of KeY Treat will be streamlined based on findings, consisting of five or fewer clinical contacts. The drug used for treatment is Epclusa®, a 12-week, once per day, pan-genotypic DAA with a favorable side effect profile. Vosevi® will also be available in cases where participants are non-responsive or are re-infected.
ARH Medical Mall, Hazard
Collaborators (1)
National Institute on Drug Abuse (NIDA)
NIH
National Cancer Institute (NCI)
NIH
Gilead Sciences
INDUSTRY
University of Kentucky
OTHER
Icahn School of Medicine at Mount Sinai
OTHER
University of Bristol
OTHER
Jennifer Havens
OTHER