drugset / Trial / NCT00558818

Long-term Study With Clevudine

NCT00558818

Phase 4 Completed 150 enrolled Bukwang Pharmaceutical
NaSingle-groupOpen-labelTreatment

Summary

A open-labeled phase lV study with 96 weeks of treatment period. The purpose of this study is to investigate safety and efficacy of clevudine in patients chronically infected with hepatitis B virus, HBeAg positive or negative.

Timeline

Start
2007-06
Primary completion
2011-09
Completion
2011-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Clevudine Small molecule 30 mg