The Immune Responses After Hepatitis B Revaccination Doses in a Young Cohort (IRHBRVD)
Primary Purpose
Hepatitis B, Vaccination; Infection, Preventable Disease, Vaccine
Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
recombinant hepatitis B vaccine
Sponsored by
About this trial
This is an interventional prevention trial for Hepatitis B focused on measuring hepatitis B vaccine, revaccination, young adult, booster
Eligibility Criteria
Inclusion Criteria:
- The actual age at the time of admission was higher than 20 years old and birth year after 1987
- Born in Taiwan and had received a full course of hepatitis B vaccines at least three doses at infant period.
- Those who have tested negative for hepatitis B surface antibody and surface antigen at baseline
- Have never been vaccinated against hepatitis B in childhood and adolescence by questionnaire
- Consent to administer 1-2 doses of hepatitis B vaccine according to the assigned group after sharing decision making process
- In good health
Exclusion Criteria:
- Those who were previously allergic to hepatitis B vaccine or its components (such as yeast)
- Those who have been vaccinated against hepatitis B during childhood and adolescence
- Those who have a positive test for hepatitis B surface antibody or a positive test for hepatitis B surface antigen
Sites / Locations
- Family Medicine, NTUHRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Active Comparator
Active Comparator
Active Comparator
Arm Label
Low titer with two doses of HB Vaccines
Low titer with one dose of HB Vaccine
Extremely low titer with two doses of HB Vaccines
Extremely low titer with one dose of HB Vaccine
Arm Description
anti-HBs titer 2.5-10 mIU/mL with two doses of HB Vaccines at Day 0 and Day 28
anti-HBs titer 2.5-10 mIU/mL with one dose of HB Vaccine at Day 0
anti-HBs titer lower than 2.5 mIU/mL with two doses of HB Vaccines at Day 0 and Day 28
anti-HBs titer lower than 2.5 mIU/mL with one dose of HB Vaccine at Day 0
Outcomes
Primary Outcome Measures
anti-HBs titer response rate at 7-10 days
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
anti-HBs titer response rate at one month
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
anti-HBs titer response rate at 6 months
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
anti-HBs titer response rate at 12 months
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
anti-HBs titer immune response change at 12 months
anti-HBs titer immune response change at 12 months after 1-2 doses of hepatitis B vaccine(s)
Secondary Outcome Measures
Full Information
NCT ID
NCT04970836
First Posted
July 6, 2021
Last Updated
June 24, 2022
Sponsor
National Taiwan University Hospital
Collaborators
Academia Sinica, Taiwan, Ministry of Science and Technology, Taiwan
1. Study Identification
Unique Protocol Identification Number
NCT04970836
Brief Title
The Immune Responses After Hepatitis B Revaccination Doses in a Young Cohort
Acronym
IRHBRVD
Official Title
The Immune Responses After Hepatitis B Revaccination Doses in a Young Cohort
Study Type
Interventional
2. Study Status
Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
July 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital
Collaborators
Academia Sinica, Taiwan, Ministry of Science and Technology, Taiwan
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This prospective cohort study aims to provide the evidence-based clinical guide to help decide the revaccination doses of hepatitis B vaccine that the high-risk young adults without hepatitis B seroprotective antibodies (anti-HBs titer<10 mIU/mL) need to take.
Detailed Description
Purpose For young adults born after the neonatal hepatitis B immunization program, especially those who were 20-33 years old after 1987, additional hepatitis B vaccination may have the benefit of strengthening protection from acute hepatitis B infection among high-risk groups. However, how many doses are most appropriate for the protection of high-risk groups is still an issue to be resolved. This study aims to provide the evidence-based clinical guide to help decide the revaccination doses of hepatitis B vaccine that the high-risk young adults without hepatitis B seroprotective antibodies (anti-HBs titer<10 mIU/mL) need to take.
Materials and Methods From August 2021 to July 2024, the investigator will invite young adults born in Taiwan over the age of 20 and born after 1987, who have received a full course of hepatitis B vaccine at least three doses at their infant period. Those who are all negative for hepatitis B surface antibodies (anti-HBs) and surface antigens (HBsAg) are enrolled to 4 groups according to the anti-HBs titer concentration (anti-HBs titer between 2.5-10 mIU/mL is a low concentration, anti-HB titer less than 2.5 mIU/mL is an extreme low concentration) with one or two doses of hepatitis B vaccine (Engerix-B) administered, respectively. Each group recruits 60 cases to reach a total of 240 participants. Each participant was followed for 12 months, and the anti-HBs titer concentration was measured in 0, 7-10 days, 28 days, 24- 28 weeks, and 48-52 weeks. The investigator will calculate the anti-HBs titer reaction rate and immune response after receiving hepatitis B vaccine(s) at each stage, and do further univariate and multivariate analysis.
Expected Results This prospective cohort study can help understand the difference in the anti-HBs titer response after 1 or 2 revaccination doses by the anti-HBs titer concentration as well as the two different types of hepatitis B vaccination in childhood It is expected to provide an important reference for the administration of hepatitis B vaccine in young adults of high-risk groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B, Vaccination; Infection, Preventable Disease, Vaccine
Keywords
hepatitis B vaccine, revaccination, young adult, booster
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
prospective cohort study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
240 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Low titer with two doses of HB Vaccines
Arm Type
Experimental
Arm Description
anti-HBs titer 2.5-10 mIU/mL with two doses of HB Vaccines at Day 0 and Day 28
Arm Title
Low titer with one dose of HB Vaccine
Arm Type
Active Comparator
Arm Description
anti-HBs titer 2.5-10 mIU/mL with one dose of HB Vaccine at Day 0
Arm Title
Extremely low titer with two doses of HB Vaccines
Arm Type
Active Comparator
Arm Description
anti-HBs titer lower than 2.5 mIU/mL with two doses of HB Vaccines at Day 0 and Day 28
Arm Title
Extremely low titer with one dose of HB Vaccine
Arm Type
Active Comparator
Arm Description
anti-HBs titer lower than 2.5 mIU/mL with one dose of HB Vaccine at Day 0
Intervention Type
Biological
Intervention Name(s)
recombinant hepatitis B vaccine
Other Intervention Name(s)
Engerix-B
Intervention Description
Hepatitis B vaccine (Engerix-B) will be administered to the eligible participants by 4 groups. Each case will be tracked for 12 months, at 0, 7-10 days, 28 days, 24-28 weeks, 48-52 weeks anti-HBs titer concentration and 4 follow-up questionnaires.
Primary Outcome Measure Information:
Title
anti-HBs titer response rate at 7-10 days
Description
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
Time Frame
7-10 days
Title
anti-HBs titer response rate at one month
Description
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
Time Frame
28 days
Title
anti-HBs titer response rate at 6 months
Description
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
Time Frame
24-28 weeks
Title
anti-HBs titer response rate at 12 months
Description
the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)
Time Frame
48-52 weeks
Title
anti-HBs titer immune response change at 12 months
Description
anti-HBs titer immune response change at 12 months after 1-2 doses of hepatitis B vaccine(s)
Time Frame
48-52 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
36 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
The actual age at the time of admission was higher than 20 years old and birth year after 1987
Born in Taiwan and had received a full course of hepatitis B vaccines at least three doses at infant period.
Those who have tested negative for hepatitis B surface antibody and surface antigen at baseline
Have never been vaccinated against hepatitis B in childhood and adolescence by questionnaire
Consent to administer 1-2 doses of hepatitis B vaccine according to the assigned group after sharing decision making process
In good health
Exclusion Criteria:
Those who were previously allergic to hepatitis B vaccine or its components (such as yeast)
Those who have been vaccinated against hepatitis B during childhood and adolescence
Those who have a positive test for hepatitis B surface antibody or a positive test for hepatitis B surface antigen
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
CHYI-FENG JAN, MD, PHD
Phone
+886-2-23123456
Ext
66824
Email
jcf036@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
CHYI-FENG JAN, MD, PhD
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Family Medicine, NTUH
City
Taipei
ZIP/Postal Code
100
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
CHYI-FENG JAN, MD, PhD
Phone
+886-2-23123456
Ext
66824
Email
jcf036@ntuh.gov.tw
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
The Immune Responses After Hepatitis B Revaccination Doses in a Young Cohort
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