The Kentucky Viral Hepatitis Treatment Study

PHASE4CompletedINTERVENTIONAL
Enrollment

374

Participants

Timeline

Start Date

September 23, 2019

Primary Completion Date

June 30, 2025

Study Completion Date

June 30, 2025

Conditions
Hepatitis COpioid-Related DisordersInjection Drug Use
Interventions
DRUG

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.

Trial Locations (1)

41701

ARH Medical Mall, Hazard

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

National Institute on Drug Abuse (NIDA)

NIH

collaborator

National Cancer Institute (NCI)

NIH

collaborator

Gilead Sciences

INDUSTRY

collaborator

University of Kentucky

OTHER

collaborator

Icahn School of Medicine at Mount Sinai

OTHER

collaborator

University of Bristol

OTHER

lead

Jennifer Havens

OTHER