A Phase 4 interventional study of Clevudine and Adefovir dipivoxil in HBeAg(-) Chronic Hepatitis B With Compensated Liver Function, sponsored by Bukwang Pharmaceutical. Completed at 2 sites in Korea, Republic of. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2012-04-25.
Sponsored by Bukwang Pharmaceutical · Phase 4, Interventional, and Treatment
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.
2,709 studies on the registry are indexed under Hepatitis A; 142 are open to participants now.
This study's enrollment of 43 is below the median of 100 across 1,886 interventional studies indexed under Hepatitis A.
Browse Hepatitis A studies →Bukwang Pharmaceutical is the lead sponsor of 34 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria
Patient with following clinical evidence
Clevudine
Drug: Clevudine
Adefovir
Drug: Adefovir dipivoxil
30mg for 48 weeks
Also known as: Levovir
10mg for 48 weeks
Also known as: Hepsera
Proportion of patients with HBV DNA below 300copies/mL
Time frame: at week 48
The change of HBV DNA from the baseline
Time frame: at week 24, 48
Proportion of patients with HBV DNA below LOD of RT-PCR
Time frame: at week 24, 48
ALT normalization rate
Time frame: at week 24, 48
Proportion of patients with viral breakthrough during 48-week treatment period
Time frame: at week 24, 48
This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.
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Bukwang Pharmaceutical