drugset / Trial / NCT00313261

Safety and Efficacy Study of L-FMAU in Chronic HBV Patients of L-FMAU-201 Placebo Group

NCT00313261

Phase 2 Terminated Bukwang Pharmaceutical
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and antiviral activity of clevudine 30 mg QD for treatment of longer period (24 weeks) in patients chronically infected with HBV.

Timeline

Start
2003-06
Primary completion
Completion
2005-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Clevudine Small molecule 30 mg