Clinical Trials Directory

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

TypeNameDescription
DRUGSofosbuvir 400 MGSofosbuvir is a direct-acting antiviral (DAA) a nucleotide analog inhibitor of hepatitis C virus nonstructural protein 5B (NS5B)
DRUGRavidasvir 200mgRavidasvir 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.