Clinical Trials Directory

Trials / Completed

CompletedNCT00219401

Neonatal Immunization With Pneumococcal Conjugate Vaccine in Papua New Guinea

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
318 (actual)
Sponsor
Papua New Guinea Institute of Medical Research · Other Government
Sex
All
Age
1 Minute – 3 Days
Healthy volunteers
Accepted

Summary

The National Health Plan 2001-2010 calls for investigation of the feasibility of pneumococcal vaccines for Papau New Guinea. The Papua New Guinea (PNG) Institute of Medical Research, the Telethon Institute for Child Health Research and the Department of Paediatrics, University of Western Australia will collaborate to examine very closely the safety of neonatal vaccination, particularly with regard to impact on the development of immunity and response to other vaccines given to infants. This study will also provide a unique opportunity for training of PNG and Australian scientists in both countries.

Detailed description

In order to obtain the earliest possible protection against invasive pneumococcal disease, achieve optimal coverage and reduce burden of early carriage, neonatal pneumococcal conjugate vaccine (PCV) immunization needs to be considered. This study in the PNG highlands will enrol 312 infants at birth, who will be randomised to receive PCV either at 1-2-3 months (infant schedule according to PNG national EPI schedule) or 0-1-2 months of age (neonatal schedule) or receive only routine immunizations (controls). Blood samples will be taken at birth-2-3-4 months of age, pre- and post-pneumococcal polysaccharide booster (23vPPV) at 9-10 months of age (to assess immune memory) and at 18 months at study completion. Carriage will be assessed weekly for the first month of life and at regular intervals thereafter. There will be ongoing surveillance for respiratory and other diseases throughout the study. In addition to serotype-specific IgG, we will examine IgG avidity, IgG subclasses, mucosal IgA and T-cell cytokine responses to PCV and pneumococcal protein antigens. To ensure immunological safety, particularly for neonatal PCV, immune responses to concomitant vaccines and viral and environmental antigens will also be examined as well as overall T-cell maturation.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPneumococcal 7 valent conjugate vaccine (Prevenar®)Accelerated PCV vaccinaton.

Timeline

Start date
2005-05-01
Primary completion
2009-05-01
Completion
2010-05-01
First posted
2005-09-22
Last updated
2011-07-12

Locations

1 site across 1 country: Papua New Guinea

Source: ClinicalTrials.gov record NCT00219401. Inclusion in this directory is not an endorsement.