Trials / Completed
CompletedNCT00362635
Compare the Efficacy and Safety of 48-week Treatment With Clevudine 30mg Versus Lamivudine 100mg for CHB Infection
A Double-blinded and Randomised Study to Compare the Efficacy and Safety of 48-week Treatment With Clevudine 30 mg qd Versus Lamivudine 100 mg qd for Chronic Hepatitis B Infection
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 92 (estimated)
- Sponsor
- Bukwang Pharmaceutical · Industry
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the efficacy and safety of 48-week treatment with Clevudine 30 mg qd versus lamivudine 100 mg qd for chronic hepatitis B infection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Clevudine |
Timeline
- Start date
- 2006-08-01
- Primary completion
- 2011-12-01
- First posted
- 2006-08-10
- Last updated
- 2012-07-26
Locations
2 sites across 1 country: Hong Kong
Source: ClinicalTrials.gov record NCT00362635. Inclusion in this directory is not an endorsement.