Study of Glecaprevir/Pibrentasvir to Assess Safety Through Real-World Data
NCT07419347 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000
Last updated 2026-04-16
Summary
The objective of this study is to assess the safety, tolerability and effectiveness of 8-week Glecaprevir/Pibrentasvir (G/P) in participants taking either prescribed or illicit drugs.
Conditions
- Hepatitis C Virus (HCV)
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
ABBVIE INC. · AbbVie
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-02-27
- Primary Completion
- 2026-06-30
- Completion
- 2026-06-30
Countries
- Canada
Study Locations
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