Glecaprevir/Pibrentasvir Fixed-dose Combination Treatment for Acute Hepatitis C Virus Infection
Part of paid clinical trials in San Diego, California.
- Sponsor
- Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
- Study ID
- NCT04042740
- Phase
- PHASE2
- Status
- Completed
Conditions
- HIV Infection
- Hepatitis C Infection
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Glecaprevir/Pibrentasvir (G/P) — DRUGFixed-dose combination (FDC) tablets containing 100 mg of glecaprevir and 40 mg of pibrentasvir; administered as 3 tablets orally.
Study Details
The purpose of this study was to assess the efficacy of a fixed dose combination (FDC) of glecaprevir/pibrentasvir (G/P) given for 4 weeks for treatment of acute hepatitis C (HCV), with or without HIV-1 coinfection.
Key Dates
- Start date
- Nov 20, 2019
- Status verified
- Jul 2024
- Primary completion
- May 18, 2023
- Completion
- Aug 22, 2023
Study Design
- Enrollment
- 45 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Glecaprevir/Pibrentasvir (G/P)Participants were assigned to receive G/P FDC tablets to be taken orally once daily for 4 weeks (Step 1). Participants who experienced HCV re-infection, suspected relapse, virologic failure, or undefined post-treatment viremia in Step 1 were offered to enter Step 2 for re-treatment. HCV re-treatment regimens may have included G/P FDC tablets orally once daily for 8-16 weeks, or alternate regimens through clinical care.
Primary Outcome Measure
Percentage of Participants With Sustained Virologic Response at 12 Weeks Post Treatment Discontinuation (SVR12) [ Time Frame: Week 16 (12 weeks post study treatment) ]
Locations (11)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Ucsd, Avrc Crs (701) | San Diego | California | 92103 | - |
| University of California, San Francisco HIV/AIDS CRS (801) | San Francisco | California | 94110 | - |
| University of Colorado Hospital CRS (6101) | Aurora | Colorado | 80045 | - |
| Whitman-Walker Institute, Inc. CRS (31791) | Washington D.C. | District of Columbia | 20005 | - |
| Johns Hopkins Adult AIDS CRS | Baltimore | Maryland | 21287 | - |
| Massachusetts General Hospital ACTG CRS (101) | Boston | Massachusetts | 02114 | - |
| Columbia Physicians and Surgeons CRS (30329) | New York | New York | 10032 | - |
| Weill Cornell Chelsea CRS (7804) | New York | New York | 10010 | - |
| Weill Cornell Upton CRS (7803) | New York | New York | 10065 | - |
| Unc Aids Crs (3201) | Chapel Hill | North Carolina | 27514 | - |
| University of Washington AIDS CRS (1401) | Seattle | Washington | 98104 | - |
Find similar trials in San Diego, CA
By condition
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Ucsd, Avrc Crs (701)· San Diego, CAUniversity of California, San Francisco HIV/AIDS CRS (801)· San Francisco, CAUniversity of Colorado Hospital CRS (6101)· Aurora, COWhitman-Walker Institute, Inc. CRS (31791)· Washington D.C., DCJohns Hopkins Adult AIDS CRS· Baltimore, MDMassachusetts General Hospital ACTG CRS (101)· Boston, MA
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