drugset / Trial / NCT04042740
Glecaprevir/Pibrentasvir Fixed-dose Combination Treatment for Acute Hepatitis C Virus Infection
Phase 2
Completed
45 enrolled
Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
AbbVie · collabNational Institute of Allergy and Infectious Diseases (NIAID) · collab
NaSingle-groupOpen-labelTreatment
Summary
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.
Timeline
- Start
- 2019-11-20
- Primary completion
- 2023-05-18
- Completion
- 2023-08-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | glecaprevir | Other / unclassified | 100 mg | Oral |
| Subject | pibrentasvir | Other / unclassified | 40 mg | Oral |