Trials / Completed
CompletedNCT04885855
8- Versus 12-week of Sofosbuvir-ravidasvir Treatment of Chronic Hepatitis C
Efficacy and Safety of 8- Versus 12-week Sofosbuvir-ravidasvir Treatment of Non-cirrhotic Chronic Hepatitis C Patients: An Open-label, Randomized, Multicenter Study in Malaysia
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 322 (actual)
- Sponsor
- Muhammad Radzi Abu Hassan · Other Government
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
This is open-label, randomized, multicentre study to compare the efficacy and safety of the 8-week versus 12-week of SOF-RVD combination treatment for non-cirrhotic chronic hepatitis C patients. All the recruited subjects will receive the treatment accordingly and be followed up for 24 weeks following the completion of treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Sofosbuvir 400 MG | Sofosbuvir is a direct-acting antiviral (DAA) a nucleotide analog inhibitor of hepatitis C virus nonstructural protein 5B (NS5B) |
| DRUG | Ravidasvir 200mg | Ravidasvir is an investigational direct-acting antiviral (DAA) a nucleotide analog inhibitor of hepatitis C virus nonstructural protein 5A (NS5A) |
Timeline
- Start date
- 2021-03-23
- Primary completion
- 2023-12-29
- Completion
- 2024-03-15
- First posted
- 2021-05-13
- Last updated
- 2025-03-13
Locations
1 site across 1 country: Malaysia
Source: ClinicalTrials.gov record NCT04885855. Inclusion in this directory is not an endorsement.