Status:
COMPLETED
Study Evaluating 13-valent Pneumococcal Conjugate Vaccine Catch-Up Regimens in Older Infants and Children
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Conditions:
Pneumococcal Infections
Eligibility:
All Genders
7-5 years
Phase:
PHASE3
Brief Summary
The purpose of this study is to assess the safety, tolerability and immunogenicity of a 13-valent Pneumococcal conjugate vaccine (13vPnC) in older infants and children who have not previously been imm...
Eligibility Criteria
Inclusion
- Aged from 7 months to \<72 months at time of enrollment.
- Available for entire study period and whose parent/legal guardian could be reached by telephone.
- Healthy as determined by medical history, physical examination, and judgment of the investigator.
- Parent/legal guardian had to be able to complete all relevant study procedures during subject participation.
Exclusion
- Previous vaccination with licensed or investigational pneumococcal vaccine.
- A previous anaphylactic reaction to any vaccine or vaccine-related component.
- Contraindication to vaccination with pneumococcal vaccine.
- Bleeding diathesis or condition associated with prolonged bleeding time that would contraindicate intramuscular injection.
- Known or suspected immune deficiency or suppression.
- History of culture-proven invasive disease caused by S pneumoniae.
- Major known congenital malformation or serious chronic disorders.
- Significant neurological disorder or history of seizure including febrile seizure, or significant stable or evolving disorders such as cerebral palsy, encephalopathy, hydrocephalus, or other significant disorders. Does not include resolving syndromes due to birth trauma such as Erb palsy.
- Receipt of blood products or gamma-globulin (including monoclonal antibodies) in the last 3 months.
- Participation in another investigational or interventional trial. Participation in purely observational studies is acceptable.
- Child is a direct descendant (child or grandchild) of a member of the study site personnel.
Key Trial Info
Start Date :
July 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 1 2008
Estimated Enrollment :
355 Patients enrolled
Trial Details
Trial ID
NCT00452452
Start Date
July 1 2007
End Date
March 1 2008
Last Update
August 15 2012
Active Locations (9)
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1
Bydgoszcz, Poland, 85-168
2
Bydgoszcz, Poland, 85-316
3
Dębica, Poland, 39-200
4
Krakow, Poland, 31-503