Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
90

Summary

Conditions
  • Hepatitis C
  • Renal Failure Chronic
Type
Interventional
Phase
Phase 4
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Between 21 years and 65 years
Gender
Both males and females

Description

The study objective is to determine if the administration of the direct acting antiviral glecaprevir/pibrentasvir for 8 weeks after kidney transplantation is both safe and effective at preventing the spread of HCV infection from donor kidney with known HCV infection (all genotypes) to an HCV negativ...

The study objective is to determine if the administration of the direct acting antiviral glecaprevir/pibrentasvir for 8 weeks after kidney transplantation is both safe and effective at preventing the spread of HCV infection from donor kidney with known HCV infection (all genotypes) to an HCV negative recipient as evidenced by a negative HCV viral RNA at 12 weeks post treatment.

Tracking Information

NCT #
NCT03781726
Collaborators
  • AbbVie
  • University of Pennsylvania
  • Johns Hopkins University
  • University of Cincinnati
  • Weill Medical College of Cornell University
  • University of Michigan
  • Northwestern University
Investigators
Principal Investigator: Raymond T Chung, MD Massachusetts General Hospital