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Adolescents' Response to Hepatitis B Vaccine Booster Dose (REACH)

Primary Purpose

Hepatitis B

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
hepatitis B vaccine
hepatitis B vaccine
Sponsored by
Baylor College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatitis B focused on measuring hepatitis B vaccine, duration of protection, adolescent immunization, anamnestic response, booster dose, Immunity to hepatitis B as measured by anti-HBSAg titers

Eligibility Criteria

16 Years - 19 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 16-19 years of age
  • born in the United States
  • received the full hepatitis B vaccination series by 12 months of age
  • received the third dose of hepatitis B vaccine within 10 months of the first dose

Exclusion Criteria:

  • a history of hepatitis B disease
  • being born to a mother with hepatitis B at the time of the participant's birth
  • having received hepatitis B immune globulin as an infant
  • immunosuppression including HIV or chronic/current steroid use (use > 10 days duration within the 3 months of enrollment)
  • renal insufficiency or dialysis
  • pregnancy (due to theoretical risk of different immune response among pregnant females)
  • ever receiving a booster (fourth) dose of hepatitis B vaccine
  • history of allergy to the hepatitis B vaccine
  • receipt of blood products or IgG within 3 months of enrollment
  • having received another vaccine within 2 weeks of enrollment

Sites / Locations

  • Texas Children's HospitalRecruiting
  • Texas Children's Pediatric AssociatesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

birth, lower dose booster

birth, higher dose booster

4 weeks, lower dose booster

4 weeks, higher dose booster

Arm Description

Adolescents who received their first dose of hepatitis B vaccine at or before day 7 of life who received a 10 ug dose of hepatitis B vaccine as a booster

Adolescents who received their first dose of hepatitis B vaccine at or before day 7 of life who received a 20 ug dose of hepatitis B vaccine as a booster

Adolescents who received their first dose of hepatitis B vaccine at or after 4 weeks of life who received a 10 ug dose of hepatitis B vaccine as a booster

Adolescents who received their first dose of hepatitis B vaccine at or after 4 weeks of life who received a 20 ug dose of hepatitis B vaccine as a booster

Outcomes

Primary Outcome Measures

anti-HBSAg titers

Secondary Outcome Measures

Full Information

First Posted
April 22, 2011
Last Updated
April 22, 2011
Sponsor
Baylor College of Medicine
Collaborators
Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT01341275
Brief Title
Adolescents' Response to Hepatitis B Vaccine Booster Dose
Acronym
REACH
Official Title
Project to Evaluate Hepatitis B Vaccine-induced Immunity Among US-born Adolescents Who Received Hepatitis B Primary Vaccination Series During Early Childhood
Study Type
Interventional

2. Study Status

Record Verification Date
April 2011
Overall Recruitment Status
Unknown status
Study Start Date
April 2010 (undefined)
Primary Completion Date
November 2011 (Anticipated)
Study Completion Date
November 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Baylor College of Medicine
Collaborators
Centers for Disease Control and Prevention

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aims of this study are to determine: the degree of immunity against hepatitis B, factors associated with immunity against hepatitis B, if the amount of antigen provided in a booster dose (used to measure the degree of immune memory) affects the body's response to the booster, and if the age at which the vaccination was initiated during infancy affects duration of protection against hepatitis B among adolescents 16-19 years of age born in the United States who were immunized against hepatitis B as infants. These data will be important to evaluate the potential need for a possible booster dose of hepatitis B vaccine among adolescents. Study subjects eligible for enrollment will: have blood drawn for baseline serologies receive the hepatitis B booster dose (randomly determined to be either a 10 ug or 20 ug dose) have blood drawn again 14 days later to determine if the booster dose has engendered an anamnestic response (a response attributed to prior immunity rather than a new response to the vaccine) The primary hypothesis is that the majority of young people will exhibit immune memory for hepatitis B in response to a booster dose of vaccine.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B
Keywords
hepatitis B vaccine, duration of protection, adolescent immunization, anamnestic response, booster dose, Immunity to hepatitis B as measured by anti-HBSAg titers

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
birth, lower dose booster
Arm Type
Experimental
Arm Description
Adolescents who received their first dose of hepatitis B vaccine at or before day 7 of life who received a 10 ug dose of hepatitis B vaccine as a booster
Arm Title
birth, higher dose booster
Arm Type
Experimental
Arm Description
Adolescents who received their first dose of hepatitis B vaccine at or before day 7 of life who received a 20 ug dose of hepatitis B vaccine as a booster
Arm Title
4 weeks, lower dose booster
Arm Type
Experimental
Arm Description
Adolescents who received their first dose of hepatitis B vaccine at or after 4 weeks of life who received a 10 ug dose of hepatitis B vaccine as a booster
Arm Title
4 weeks, higher dose booster
Arm Type
Experimental
Arm Description
Adolescents who received their first dose of hepatitis B vaccine at or after 4 weeks of life who received a 20 ug dose of hepatitis B vaccine as a booster
Intervention Type
Biological
Intervention Name(s)
hepatitis B vaccine
Other Intervention Name(s)
EngerixB
Intervention Description
10 ug dose, one-time administration
Intervention Type
Biological
Intervention Name(s)
hepatitis B vaccine
Other Intervention Name(s)
EngerixB
Intervention Description
20 ug dose, one-time administration
Primary Outcome Measure Information:
Title
anti-HBSAg titers
Time Frame
13-15 days after enrollment and booster dose

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 16-19 years of age born in the United States received the full hepatitis B vaccination series by 12 months of age received the third dose of hepatitis B vaccine within 10 months of the first dose Exclusion Criteria: a history of hepatitis B disease being born to a mother with hepatitis B at the time of the participant's birth having received hepatitis B immune globulin as an infant immunosuppression including HIV or chronic/current steroid use (use > 10 days duration within the 3 months of enrollment) renal insufficiency or dialysis pregnancy (due to theoretical risk of different immune response among pregnant females) ever receiving a booster (fourth) dose of hepatitis B vaccine history of allergy to the hepatitis B vaccine receipt of blood products or IgG within 3 months of enrollment having received another vaccine within 2 weeks of enrollment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amy B Middleman, MD
Phone
832-822-3664
Email
amym@bcm.edu
Facility Information:
Facility Name
Texas Children's Hospital
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting
Facility Name
Texas Children's Pediatric Associates
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Individual Site Status
Recruiting

12. IPD Sharing Statement

Citations:
PubMed Identifier
25643863
Citation
Spradling PR, Kamili S, Xing J, Drobeniuc J, Hu DJ, Middleman AB. Response to challenge dose among young adults vaccinated for hepatitis B as infants: importance of detectable residual antibody to hepatitis B surface antigen. Infect Control Hosp Epidemiol. 2015 May;36(5):529-33. doi: 10.1017/ice.2015.6. Epub 2015 Feb 3.
Results Reference
derived
PubMed Identifier
24843060
Citation
Middleman AB, Baker CJ, Kozinetz CA, Kamili S, Nguyen C, Hu DJ, Spradling PR. Duration of protection after infant hepatitis B vaccination series. Pediatrics. 2014 Jun;133(6):e1500-7. doi: 10.1542/peds.2013-2940. Epub 2014 May 19.
Results Reference
derived

Learn more about this trial

Adolescents' Response to Hepatitis B Vaccine Booster Dose

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