Overview

Safety and Antiviral Activity Study of Clevudine 30 mg QD in Patient With Chronic HBV

Status:
Terminated
Trial end date:
2004-11-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to determine safety and efficacy of 30 mg daily dose of clevudine (L-FMAU) at 24 weeks of treatment in patients with chronic HBV.
Phase:
Phase 3
Details
Lead Sponsor:
Bukwang Pharmaceutical
Treatments:
Antiviral Agents
Clevudine