drugset / Trial / NCT00313287

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

NCT00313287

Phase 3 Terminated 180 enrolled Bukwang Pharmaceutical
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2003-06
Primary completion
Completion
2004-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Clevudine Small molecule 30 mg