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A Study to Evaluate the Reactogenicity, Safety, and Immunogenicity of the Third Generation Hepatitis B Vaccine

Primary Purpose

Healthy

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
CVI-HBV-001
Conventional Hepatitis B vaccine (20 μg)
Sponsored by
CHA Vaccine Institute Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Healthy

Eligibility Criteria

20 Years - 50 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Adults between 20 and 50 years of age
  2. Anti-HBs titers < 10 mIU/mL
  3. Subject is able to provide written informed consent by oneself or legal representative

Exclusion Criteria:

  1. Hepatitis B core antibodies positive patient
  2. Patient has abnormal results in liver-function test
  3. Patient has active microbial, viral, or fungal infections in need of systemic treatment
  4. Patient has history of serious heart disease (NYHA Functional Class III or IV heart failure, myocardial infarction within 6 months, treatment required ventricular tachyarrhythmias, or unstable angina etc.)
  5. Patient has seizure disorder required anticonvulsants treatment
  6. Serious chronic obstructive pulmonary disease patient accompanied hypoxemia
  7. Uncontrollable diabetic patient
  8. Uncontrollable hypertension patient
  9. Patient with known history of HIV, HBV, or HCV infection
  10. Subject had experience of participating other clinical study or clinical treatment within 30 days before screening
  11. Subject has hypersensitivity or anaphylactic reaction for HBV vaccine components
  12. Patient being treated for prolonged immunosuppressive therapy (including steroids)
  13. Hemodialysis patient
  14. Subject has continuous drinking (>21 units/week, 1 unit = 10g of pure alcohol) or dependence on alcohol
  15. Subject is pregnant or breastfeeding or intending to become pregnant during the study
  16. Subject has any other significant findings unacceptable in this study under the opinion of the investigator

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm 5

    Arm Type

    Experimental

    Experimental

    Experimental

    Experimental

    Active Comparator

    Arm Label

    CVI-HBV-001 (5 μg)

    CVI-HBV-001 (10 μg)

    CVI-HBV-001 (20 μg)

    CVI-HBV-001 (40 μg)

    Conventional Hepatitis B vaccine (20 μg)

    Arm Description

    HBV surface antigen 5 μg/dose Intramuscular injection at 0, 1, 6th month

    HBV surface antigen 10 μg/dose Intramuscular injection at 0, 1, 6th month

    HBV surface antigen 20 μg/dose Intramuscular injection at 0, 1, 6th month

    HBV surface antigen 40 μg/dose Intramuscular injection at 0, 1, 6th month

    HBV surface antigen 20 μg/dose Intramuscular injection at 0, 1, 6th month

    Outcomes

    Primary Outcome Measures

    Safety and reactogenicity (including incidence of adverse events and expected adverse reactions for vaccine treatment) measured for 7 days after each vaccination
    Occurrence of severe local and/or systemic reactogenicity signs and symptoms measured for 7 days after each vaccination

    Secondary Outcome Measures

    Seroprotection rate
    Seroprotection (> 10 mIU/mL of anti-HBs) rate measured 4 weeks after vaccination
    Antibody titers to HBsAg
    Geometric mean titer (GMT, mIU/mL) measured 4 weeks after vaccination

    Full Information

    First Posted
    February 18, 2016
    Last Updated
    February 22, 2016
    Sponsor
    CHA Vaccine Institute Co., Ltd.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02692170
    Brief Title
    A Study to Evaluate the Reactogenicity, Safety, and Immunogenicity of the Third Generation Hepatitis B Vaccine
    Official Title
    A Single Center, Randomized, Double Blinded PhaseI/IIa Exploratory Study to Evaluate Reactogenicity, Safety, Immunogenicity and Dose Response of a New Hepatitis B Vaccine in Human Adult
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2016
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2012 (undefined)
    Primary Completion Date
    June 2015 (Actual)
    Study Completion Date
    June 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    CHA Vaccine Institute Co., Ltd.

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    A single center, randomized, double blinded phase I/IIa exploratory study to evaluate reactogenicity, safety, immunogenicity and dose-response of a new hepatitis B vaccine in human adult
    Detailed Description
    Objectives: To explore the most effective dose of the third generation Hepatitis B vaccine through the evaluation of reactogenicity, safety, and immunogenicity. Subjects: Adults having anti-HBs antibody titers less than 10 mIU/mL after 3 previous injections of the conventional Hepatitis B vaccine. Study hypothesis: The third generation Hepatitis B vaccine, containing preS antigens in addition to S antigen, has an ability to elicit faster protection and higher antibody titers than the second generation Hepatitis B vaccine in the subjects.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Healthy

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 1, Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    75 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    CVI-HBV-001 (5 μg)
    Arm Type
    Experimental
    Arm Description
    HBV surface antigen 5 μg/dose Intramuscular injection at 0, 1, 6th month
    Arm Title
    CVI-HBV-001 (10 μg)
    Arm Type
    Experimental
    Arm Description
    HBV surface antigen 10 μg/dose Intramuscular injection at 0, 1, 6th month
    Arm Title
    CVI-HBV-001 (20 μg)
    Arm Type
    Experimental
    Arm Description
    HBV surface antigen 20 μg/dose Intramuscular injection at 0, 1, 6th month
    Arm Title
    CVI-HBV-001 (40 μg)
    Arm Type
    Experimental
    Arm Description
    HBV surface antigen 40 μg/dose Intramuscular injection at 0, 1, 6th month
    Arm Title
    Conventional Hepatitis B vaccine (20 μg)
    Arm Type
    Active Comparator
    Arm Description
    HBV surface antigen 20 μg/dose Intramuscular injection at 0, 1, 6th month
    Intervention Type
    Biological
    Intervention Name(s)
    CVI-HBV-001
    Intervention Description
    Investigational product: CVI-HBV-001 Dose: 5, 10, 20 or 40ug Frequency: 3 times Vaccination schedule: at 0, 1, 6 months Administration route: Intramuscular injection
    Intervention Type
    Biological
    Intervention Name(s)
    Conventional Hepatitis B vaccine (20 μg)
    Intervention Description
    Active comparator: Conventional Hepatitis B vaccine (20 μg) Dose: 20ug Frequency: 3 times Vaccination schedule: at 0, 1, 6 months Administration route: Intramuscular injection
    Primary Outcome Measure Information:
    Title
    Safety and reactogenicity (including incidence of adverse events and expected adverse reactions for vaccine treatment) measured for 7 days after each vaccination
    Description
    Occurrence of severe local and/or systemic reactogenicity signs and symptoms measured for 7 days after each vaccination
    Time Frame
    7 days after each vaccination
    Secondary Outcome Measure Information:
    Title
    Seroprotection rate
    Description
    Seroprotection (> 10 mIU/mL of anti-HBs) rate measured 4 weeks after vaccination
    Time Frame
    4 weeks after vaccination
    Title
    Antibody titers to HBsAg
    Description
    Geometric mean titer (GMT, mIU/mL) measured 4 weeks after vaccination
    Time Frame
    4 weeks after vaccination

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    20 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Adults between 20 and 50 years of age Anti-HBs titers < 10 mIU/mL Subject is able to provide written informed consent by oneself or legal representative Exclusion Criteria: Hepatitis B core antibodies positive patient Patient has abnormal results in liver-function test Patient has active microbial, viral, or fungal infections in need of systemic treatment Patient has history of serious heart disease (NYHA Functional Class III or IV heart failure, myocardial infarction within 6 months, treatment required ventricular tachyarrhythmias, or unstable angina etc.) Patient has seizure disorder required anticonvulsants treatment Serious chronic obstructive pulmonary disease patient accompanied hypoxemia Uncontrollable diabetic patient Uncontrollable hypertension patient Patient with known history of HIV, HBV, or HCV infection Subject had experience of participating other clinical study or clinical treatment within 30 days before screening Subject has hypersensitivity or anaphylactic reaction for HBV vaccine components Patient being treated for prolonged immunosuppressive therapy (including steroids) Hemodialysis patient Subject has continuous drinking (>21 units/week, 1 unit = 10g of pure alcohol) or dependence on alcohol Subject is pregnant or breastfeeding or intending to become pregnant during the study Subject has any other significant findings unacceptable in this study under the opinion of the investigator
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Seong Gyu Hwang, M.D., Ph.D.
    Organizational Affiliation
    Bundang CHA General Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    A Study to Evaluate the Reactogenicity, Safety, and Immunogenicity of the Third Generation Hepatitis B Vaccine

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