Chronic Hepatitis B Clinical Trial
Official title:
Second Stage:Open-label Study of Therapeutic Hepatitis B Vaccine (Mimogen-based) in Treating Chronic Hepatitis B Patients
The purpose is to evaluate efficacy and safety of therapeutic HBV vaccine (mimogen-based) treatment in chronic hepatitis B patients and to explore the most effective dosage and provide the rational for optimal dosing schedule.
Second stage(76-144 weeks):
In this follow-up stage the trial is open designed, and all the subjects completed the first
stage study(0-76 weeks)
1. Subjects with virological response but no serological response/with serological response
but no virological response/neither virological nor serological response in the first
stage, and be willing to continue the this follow-up study, will be treated by εPA-44
900 μg at week 80,83,86,89,92,95,98,101,104,108,112,116,120,124,128.
2. Subjects with both virological and serological response, will be followed-up to 144
weeks with no Adefovir Dipivoxil or εPA-44 900 μg treatment.
The definition of response as below:
1. Virological response: HBV DNA<2.93×10∧3IU/ml at 76 weeks;
2. Serological response: serological conversion of HBeAg at 76 weeks.
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