drugset / Trial / NCT00313274

Safety and Antiviral Activity Study of Clevudine 30 mg QD in Patients With HBeAg(-) Chronic HBV

NCT00313274

Phase 3 Terminated 80 enrolled Bukwang Pharmaceutical
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine safety and efficacy of 30mg daily dose of clevudine (L-FMAU) at 24 weeks of treatment in chronic HBV infected patients with HBeAg negative

Timeline

Start
2003-07
Primary completion
Completion
2004-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Clevudine Small molecule 30 mg