Clinical Trials Directory

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

TypeNameDescription
DRUGClevudine

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.

Compare the Efficacy and Safety of 48-week Treatment With Clevudine 30mg Versus Lamivudine 100mg for CHB Infection (NCT00362635) · Clinical Trials Directory