Lead Sponsor

Sanofi

Age

0 - 0 years

Sex

ALL

Healthy Volunteers

Yes

•Healthy infants 2 months (≥ 42 days and ≤ 89 days) of age.
•Infants with at least 36 weeks of gestation at delivery.
•Must have received 1 dose of Hepatitis B vaccine (with that dose at least 15 days before the administration of study vaccines).
•Able to attend the scheduled visits and to comply with the study procedures.
•Parent or legal guardian willing to take rectal temperatures during the infant series.
•Parent or legal guardian has access to a telephone.
•Signed informed consent from parent or legal guardian obtained before the 1st study intervention.
•Able to obtain at least 1.5 mL of blood sample prior to Dose 1.

•Clinically significant findings on review of systems (determined by investigator or sub-investigator to be sufficient for exclusion).
•Known or suspected hypersensitivity to any component of the study vaccine to be administered.
•Known or suspected impairment of immunologic function or receipt of immunosuppressive therapy or immunoglobulin since birth.
•Known Human Immunodeficiency Virus (HIV)-positive mother or child.
•Personal or immediate family history of congenital immune deficiency.
•Developmental delay or neurologic disorder.
•Chronic medical, congenital, or developmental disease.
•Participation in any other clinical trial.
•Any condition which, in the opinion of the investigator, would interfere with the evaluation of the vaccine or pose a health risk to the subject.
•Prior history of having received any Acellular Pertussis- (DTaP) or Whole Cell Pertussis- (DTwP) based combination vaccines, Haemophilus influenzae Type b (Hib)-conjugate, Poliovirus, or Pneumococcal conjugate vaccines.

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