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Phase 2 N=378 Randomized Quadruple-blind Treatment

Therapeutic Hepatitis B Vaccine (Mimogen-based) Joint Entecavir in Treating Chronic Hepatitis B Patients

Chronic Hepatitis B

Enrolled (actual)
378
Serious AEs
0.3%
Results posted
Jun 2019
Primary outcome: Primary: Percentage of Participants With HBeAg Seroconversion at Week 48 — 21; 23 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Therapeutic HBV vaccine (Biological); entecavir (Drug); placebo (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Chongqing Jiachen Biotechnology Ltd.
Primary completion
Jan 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With HBeAg Seroconversion at Week 48
21; 23
SECONDARY
Serological Response
SECONDARY
Virological Response
SECONDARY
Biochemistry Response
SECONDARY
Histological Response

Summary

The purpose is to evaluate efficacy and safety of therapeutic hepatitis B virus (HBV) vaccine (mimogen-based)) Joint entecavir treatment in chronic hepatitis B patients.

Eligibility Criteria

Inclusion Criteria

  • Aged 18-65 years, male or female;
  • Conforming to diagnosis standard of chronic hepatitis B according to " 2005 Guideline for Prevention and Treatment of Hepatitis B " , (with positive HBsAg for more than 6 months), never have systemic treatment of anti-HBV viral ,and
  • HBV-DNA ≥ 1.72×10^4 IU/ml;
  • HBeAg (+), HBeAb (-);
  • ALT within 2 to 10 times of ULN (upper limits of normal);
  • HLA-A2 positive;
  • Compensatory liver disease having following hematological and biochemical parameters:
  • WBC ≥ 3.5×10^9/L;
  • ANC ≥ 1.5×10^9/L;
  • PLT ≥ 80×10^9/L;
  • Hb ≥ 100g/L;
  • TBil ≤ 1.5 ULN;
  • ALB not lower than low limit of normal value;
  • BUN no more than high limit of normal value;
  • Cr ≤ 1.5 ULN high limit of normal value;
  • PT elongation ≤ 3 sec, APTT in normal value;
  • Fasting blood glucose ≤ 7.0mmol/L;
  • TSH in normal value;
  • AFP test result no more than high limit of normal value;
  • Take effective contraception for subject with child-bearing potential (including females and female partners of males);
  • Understand and sign ICF approved by EC;
  • Willing to comply with the study procedures and complete the study.

Exclusion Criteria

  • Antibodies of HCV, HDV or HIV is positive;
  • ANA titer > 1:100;
  • Decompensated liver disease (such as gullet and pylorus varicose veins, hepatic encephalopathy);
  • Have the following illness or with severe disease inappropriate to participate in the study in the view of the investigator, in cardiovascular system: instable or significant cardiovascular illness such as angina pectoris, heart attack of myocardial infarction, congestive heart failure, severe hypertension, significant arrhythmia or abnormal ECG etc;
  • Respiratory system: bronchiectasia, bronchial asthma, chronic obstructive pulmonary disease, respiratory failure, etc;
  • Endocrine, metabolism diseases: diabetes mellitus, uncontrolled thyroid diseases, etc;
  • Others: autoimmune disorder, active tuberculosis, malignancies (e.g.: tumor), neuropathic, metal, acute or chronic pancreatitis illness history, etc.
  • Have used anti-HBV drug ( Interferon, Lamivudine, Adefovir Dipivoxil, Entecavir and Telbivudine ) and immunomodulator ( Thymic peptide, etc ) to the administration of study medication;
  • Have allergic diathesis or have suspected allergy to εPA-44;
  • Female in pregnancy, lactation or those who plan to pregnancy during the course of the study;
  • Have history of alcohol abuse (Alcohol consumption for more than 5 years, with daily consumption over 40g for males and over 20g for females) and known drug dependence;
  • Have history of organ transplantation (except corneal transplantation and hair transplantation);
  • Have participated in any other drug clinical investigations within 3 months;
  • Any other factors inappropriate for enroll in the study or study completion in the view of the investigator.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01326546). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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