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Clinical Trial Summary

The primary purpose of this study is to evaluate the immune response to 13-valent pneumococcal conjugate vaccine (13vPnCV) in children who as infants received either a complete series of PnCV versus a combination of PnCV and pneumococcal polysaccharide vaccine (PSV). This study is also intended to evaluate the safety of the 13vPnC.


Clinical Trial Description

Follow-up measure for the EMEA supporting a Type II variation for Prevenar (PCV7) label ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00853749
Study type Interventional
Source Wyeth is now a wholly owned subsidiary of Pfizer
Contact
Status Completed
Phase Phase 3
Start date May 5, 2009
Completion date December 16, 2009

See also
  Status Clinical Trial Phase
Completed NCT00227188 - Study Evaluating Prevenar in the Prevention of Invasive Pneumococcal Disease (IPD) in the Paediatric Population in Spain. N/A
Recruiting NCT00885625 - 7-valent Pneumococcal Conjugated Vaccination Phase 4
Completed NCT04464291 - An Epidemiological Survey to Establish the Spectrum of Circulating Serotypes of S. Pneumoniae, in Patients Older 18 Years N/A
Completed NCT01128439 - Study Estimating the Impact of Prevnar 13™ (13vPnC) on Invasive Pneumococcal Disease
Completed NCT01083459 - Impact of PCV on Disease and Colonization Among Native American Communities N/A
Completed NCT00371878 - Immunogenicity of 7-Valent Pneumococcal Conjugate Vaccine in Lung Fluid of Adults With and Without HIV Infection Phase 4