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Immunogenicity Study of an Inactivated Hepatitis A Vaccine in Infants and Young Children

Primary Purpose

Hepatitis A

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
hepatitis A vaccine
Sponsored by
Centers for Disease Control and Prevention
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hepatitis A focused on measuring hepatitis A, hepatitis A vaccine

Eligibility Criteria

undefined - 6 Months (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:term infant with normal growth and development, considered to be healthy at age 6 months; written informed consent by parent/guardian - Exclusion Criteria:received or expected to receive immune globulin or blood/blood products while enrolled; received or expected to receive immunosuppressive therapy within 30 days of vaccination or has immune deficiency; currently enrolled in another vaccine trial; progressive or unstable neurological disorder -

Sites / Locations

  • Anchorage Neighborhood Health Center
  • Alaska Native Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

HAVRIX 6 and 12 mos; mother antibody pos

HAVRIX age 6, 12 mos; mom antibody neg

HAVRIX ages 12, 15 mos; mom antibody +

HAVRIX ages 12, 15 mos; mom antibody-

HAVRIX ages 15,21 mos; mom antibody +

HAVRIX ages 15,21 mos; mom antibody -

Arm Description

HAVRIX administered to infants born to anti-HAV positive mothers at ages 6 and 12 months

HAVRIX administered to infants born to anti-HAV negative mothers at ages 6 and 12 months

HAVRIX administered to infants born to anti-HAV positive mothers at ages 12 and 15 months

HAVRIX administered to infants born to anti-HAV negative mothers at ages 12 and 15 months

HAVRIX administered to infants born to anti-HAV positive mothers at ages 15 and 21 months

HAVRIX administered to infants born to anti-HAV negative mothers at ages 15 and 21 months

Outcomes

Primary Outcome Measures

concentration of antibody to hepatitis A virus
Sera obtained at time of first hepatitis A vaccine dose (baseline) and 1, 7, and 12 months thereafter

Secondary Outcome Measures

reported side effects and adverse events
at time of each vaccine dose, parent was given a diary card on which to record systemic and injection site signs and symptoms observed on day of vaccination and subsequent 3 days.
antibodies to routine childhood vaccinations
in a sample of study subjects from each group, blood drawn at age 13 months was tested for response to routine vaccinations.

Full Information

First Posted
August 29, 2005
Last Updated
August 29, 2012
Sponsor
Centers for Disease Control and Prevention
Collaborators
Alaska Native Medical Center, GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT00139113
Brief Title
Immunogenicity Study of an Inactivated Hepatitis A Vaccine in Infants and Young Children
Official Title
Immunogenicity Study of an Inactivated Hepatitis A Vaccine in Infants and Young Children
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
September 1996 (undefined)
Primary Completion Date
June 2001 (Actual)
Study Completion Date
June 2001 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Centers for Disease Control and Prevention
Collaborators
Alaska Native Medical Center, GlaxoSmithKline

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Infants born to immune mothers and therefore having passively-transferred maternal antibody (PMA) to hepatitis A virus (HAV) have a blunted immune response to hepatitis A vaccine. We compared the immunogenicity of hepatitis A vaccine among infants with and without PMA, vaccinated on different schedules. We found that when vaccination is begun at or after 12 months of age, there was no difference in the immune response to the vaccine between infants born to immune vs. susceptible mothers.
Detailed Description
Background: Infants with passively-transferred maternal antibody (PMA) to hepatitis A virus (HAV) have a blunted immune response to hepatitis A vaccine. We compared the immunogenicity of hepatitis A vaccine among infants with and without PMA, vaccinated on different schedules. Methods: Infants were randomized to one of three groups, each receiving two doses of 720 EL.U. of hepatitis A vaccine (HAVRIX, Glaxo SmithKline) according to the following schedules: Group 1 at ages 6 and 12 months; Group 2 at ages 12 and 18 months; Group 3 at ages 15 and 21 months. We determined antibody to HAV (anti-HAV) status of mothers at the time of delivery, and measured infants' anti-HAV concentrations at the time of the first vaccine dose (baseline), and at 1, 7 and 12 months thereafter. Anti-HAV concentrations > 33 milli-International Units/milliliter (mIU/mL) were considered protective. We monitored adverse reactions using diary cards and chart reviews. Results: A total of 239 infants were enrolled, including 134 born to anti-HAV negative mothers (Groups 1N, 2N, 3N) and 105 born to anti-HAV positive mothers (Groups 1P, 2P, 3P). At month 12, 6 months after the second vaccine dose, the difference in GMC between Groups 1P and 1N was the only statistically significant difference within groups (p<0.05). There were no statistically significant differences in GMC among groups of infants born to anti-HAV negative mothers ("N" groups), but the difference between Group 1P and Group 3P infants was significant (p < 0.05). No serious adverse reactions related to vaccination were detected. Conclusions: Hepatitis A vaccine is immunogenic among infants born to anti-HAV negative mothers, and among those born to anti-HAV positive mothers and vaccinated beginning as young as 12 months old. The persistence of PMA for at least six months among the majority of infants born to anti-HAV positive mothers results in lower seroconversion rates and GMC's.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis A
Keywords
hepatitis A, hepatitis A vaccine

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
Randomized
Enrollment
248 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HAVRIX 6 and 12 mos; mother antibody pos
Arm Type
Experimental
Arm Description
HAVRIX administered to infants born to anti-HAV positive mothers at ages 6 and 12 months
Arm Title
HAVRIX age 6, 12 mos; mom antibody neg
Arm Type
Active Comparator
Arm Description
HAVRIX administered to infants born to anti-HAV negative mothers at ages 6 and 12 months
Arm Title
HAVRIX ages 12, 15 mos; mom antibody +
Arm Type
Experimental
Arm Description
HAVRIX administered to infants born to anti-HAV positive mothers at ages 12 and 15 months
Arm Title
HAVRIX ages 12, 15 mos; mom antibody-
Arm Type
Active Comparator
Arm Description
HAVRIX administered to infants born to anti-HAV negative mothers at ages 12 and 15 months
Arm Title
HAVRIX ages 15,21 mos; mom antibody +
Arm Type
Experimental
Arm Description
HAVRIX administered to infants born to anti-HAV positive mothers at ages 15 and 21 months
Arm Title
HAVRIX ages 15,21 mos; mom antibody -
Arm Type
Active Comparator
Arm Description
HAVRIX administered to infants born to anti-HAV negative mothers at ages 15 and 21 months
Intervention Type
Biological
Intervention Name(s)
hepatitis A vaccine
Other Intervention Name(s)
HAVRIX
Intervention Description
2 doses of inactivated hepatitis A vaccine manufactured by GSK in licensed pediatric formulation of 720 EL. U. per dose given on 3 different schedules: aged 6 and 12 months, 12 and 18 months, and 15 and 21 months. Within each group, subjects were randomized to achieve a relatively equal number of children born to anti-HAV positive and anti-HAV negative mothers.
Primary Outcome Measure Information:
Title
concentration of antibody to hepatitis A virus
Description
Sera obtained at time of first hepatitis A vaccine dose (baseline) and 1, 7, and 12 months thereafter
Time Frame
baseline and 1, 7, and 12 months post vax
Secondary Outcome Measure Information:
Title
reported side effects and adverse events
Description
at time of each vaccine dose, parent was given a diary card on which to record systemic and injection site signs and symptoms observed on day of vaccination and subsequent 3 days.
Time Frame
day of vaccination and 3 days thereafter
Title
antibodies to routine childhood vaccinations
Description
in a sample of study subjects from each group, blood drawn at age 13 months was tested for response to routine vaccinations.
Time Frame
age 13 months

10. Eligibility

Sex
All
Maximum Age & Unit of Time
6 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:term infant with normal growth and development, considered to be healthy at age 6 months; written informed consent by parent/guardian - Exclusion Criteria:received or expected to receive immune globulin or blood/blood products while enrolled; received or expected to receive immunosuppressive therapy within 30 days of vaccination or has immune deficiency; currently enrolled in another vaccine trial; progressive or unstable neurological disorder -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian McMahon
Organizational Affiliation
Alaska Native Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Anchorage Neighborhood Health Center
City
Anchorage
State/Province
Alaska
ZIP/Postal Code
99501
Country
United States
Facility Name
Alaska Native Medical Center
City
Anchorage
State/Province
Alaska
ZIP/Postal Code
99508
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17259872
Citation
Bell BP, Negus S, Fiore AE, Plotnik J, Dhotre KB, Williams J, Shapiro CN, McMahon BJ. Immunogenicity of an inactivated hepatitis A vaccine in infants and young children. Pediatr Infect Dis J. 2007 Feb;26(2):116-22. doi: 10.1097/01.inf.0000253253.85640.cc.
Results Reference
result

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Immunogenicity Study of an Inactivated Hepatitis A Vaccine in Infants and Young Children

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