drugset / Trial / NCT00641082

A Double-Blind Randomized Clinical Trial Comparing the Safety and Antiviral Activity of 48-week Clevudine and Adefovir Dipivoxil in HBeAg(-) Chronic Hepatitis B With Compensated Liver Function

NCT00641082

Phase 4 Completed 43 enrolled Bukwang Pharmaceutical
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A double-blind randomized, parallel, multicenter with 48 weeks of treatment period. The purpose of this study is to compare the safety and antiviral activity of 48-week Clevudine and Adefovir dipivoxil in HBeAg(-) Chronic Hepatitis B with compensated liver function.

Timeline

Start
2008-02
Primary completion
2012-03
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adefovir dipivoxil Small molecule 10 mg
Subject Clevudine Small molecule 30 mg