Immunogenicity Study of an Inactivated Hepatitis A Vaccine in Infants and Young Children
Hepatitis A
About this trial
This is an interventional prevention trial for Hepatitis A focused on measuring hepatitis A, hepatitis A vaccine
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 -
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
Experimental
Active Comparator
Experimental
Active Comparator
Experimental
Active Comparator
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 -
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