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OpenTrials
Completed

NCT Number: NCT00772928

Study of the Effect of Pneumococcal Conjugate Vaccine (PCV) on Immunogenicity of Pentacel™

This study is designed to evaluate in a controlled manner the effect of Prevnar® on the immune responses of Pentacel™

Primary Objective - Stage I:

To compare the immune responses elicited by an infant series of Pentacel™ when given at different times from or concurrently with a Pneumococcal conjugate vaccine (Prevnar®).

Primary Objective - Stage II:

To compare the immune responses elicited by a 4th dose of Pentacel™ when given at different times from or concurrently with Prevnar®.

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Key information

About this study

This is a 2-staged study. Stage I of this study is designed to compare the immune responses elicited by an infant series (3 doses) of Pentacel™ when given at different times from or concurrently with Prevnar®.

Stage II is designed to describe the immune responses elicited by a 4th dose of Pentacel™ (all antigens) when given at different times from or concurrently with Prevnar®.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Pentacel™: HCPDT-IPV//PRP-T Vaccine and Prevnar®

Biological

0.5 mL, Intramuscular

Other names: Pentacel™, Prevnar®

Primary outcomes

  1. Percentage of Participants With 4-fold Rises in Levels of Pentacel™ Vaccine Antibody Titers Post-dose 3 When Given at Different Times or Concurrently With a Pneumococcal Conjugate Vaccine (Prevnar®)

    Time frame: 28 to 48 days post-3rd vaccination

    Seroconversion was defined as the percentage of subjects with ≥ 4-fold post-dose 3 for anti-pertussis and ≥ 0.15 μg/mL or ≥ 1.0 μg/mL for anti-Polyribosylribitol Phosphate (PRP) responses.

  2. Geometric Mean Titers of Antibodies to Pertussis, Diphtheria, Tetanus, Polyribosylribitol Phosphate and Poliovirus Elicited by an Infant Series of Pentacel™ When Given at Different Times or Concurrently With a Pneumococcal Conjugate Vaccine (Prevnar®)

    Time frame: 60 Days Post-dose 3

    Anti-pertussis response include antibodies to Pertussis Toxoid (PT); Filamentous Haemagglutinin (FHA); Fimbriae Types 2 and 3 (FIM) and Pertactin (PRN) antigens.

Other outcomes

  1. Percentage of Subjects With Solicited Local, Systemic Reactions Occurring Between 0-3 Days After Each Dose of Pentacel™

    Time frame: 0-3 days post- vaccination and entire study period

    Solicited local reactions: redness, swelling, and tenderness. Solicited systemic reactions: fever (temperature), irritability post-vaccinal, crying, lethargy, appetite decreased, vomiting, diarrhea, and rash.

Sponsors and collaborators

Lead sponsor

Sanofi

Industry

Registry information

Official study title

Immunogenicity Assessment of Pentacel™ (Hybrid CP20/20/5/3DT-mIPV//PRP-T) When Given at Different Times From or Concurrently With a Pneumococcal Conjugate Vaccine

Important dates

Study start
2003
Primary completion
2006
Study completion
2006
First posted
Oct 15, 2008
Registry last updated
Feb 1, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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