Compare Immunogenicity & Safety of 2 Formulations of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine Given in Healthy Infants

GlaxoSmithKline (GSK)

Status and phase

Completed

Phase 3

Conditions

Poliomyelitis

Diphtheria

Tetanus

Hepatitis B

Acellular Pertussis

Treatments

Biological: DTPa-HBV-IPV/Hib vaccine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00320463

105910

Details and patient eligibility

About

In this study, infants will be randomly allocated into three groups:

one group of subjects will receive DTPa-HBV-IPV/Hib vaccine (new formulation)
the second group of subjects will receive DTPa-HBV-IPV/Hib vaccine (current formulation)
the third group of subjects will receive DTPa-HBV-IPV vaccine The study will be double-blind for the two groups receiving the DTPa-HBV-IPV/Hib vaccine (new or current formulation). The study will be single-blind for the group receiving DTPa-HBV-IPV vaccine.

Full description

A study to compare the immunogenicity & safety of 2 formulations of GlaxoSmithKline (GSK) Biologicals' DTPa-HBV-IPV/Hib vaccine given in healthy infants at 3,4 & 5 months age. The immunogenicity & safety of DTPa-HBV-IPV vaccine will also be evaluated in a 3rd group of subjects Subjects in the group that will receive DTPa-HBV-IPV/Hib vaccine (current formulation) will be the control group for the group that will receive DTPa-HBV-IPV/Hib vaccine (new formulation)

Sex

All

Ages

11 to 17 weeks old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

"Inclusion criteria:

A healthy male or female infant between, and including, 11 and 17 weeks of age at the time of the first vaccination.
Infant born to known hepatitis B surface antigen (HBsAg) seronegative mother (documented laboratory result of HBsAg assay from the maternal blood sample is available).
Born after a normal gestation period (between 36 and 42 weeks).
Written informed consent obtained from the parent or guardian of the subject.

Exclusion criteria:

Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine(s) within 30 days preceding the first dose of study vaccine, or planned use during the study period.
Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first vaccine dose.
Any chronic drug therapy to be continued during the study period.
Planned administration/ administration of a vaccine not foreseen by the study protocol during the period starting from 30 days before each dose of study vaccine and ending 30 days after the last vaccine dose.
Previous vaccination against diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B and/or Haemophilus influenzae diseases.
Known history of or exposure to diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B and/or Haemophilus influenzae diseases since birth.
History of allergic disease or reactions likely to be exacerbated by any component of the vaccines.