Clinical Trials Directory

Trials / Completed

CompletedNCT01128426

Postlicensure Observational Safety Study of 13vPnC Administered to Infants and Toddlers

Postlicensure Observational Safety Study of 13-valent Pneumococcal Conjugate Vaccine (13vPnC) Administered in Routine Use to Infants and Toddlers

Status
Completed
Phase
Study type
Observational
Enrollment
53,902 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
2 Months – 3 Years
Healthy volunteers
Accepted

Summary

The purpose of the study is to expand the understanding of the safety profile of 13vPnC in routine use following licensure and introduction of the vaccine.

Conditions

Interventions

TypeNameDescription
OTHERNo InterventionNo Intervention

Timeline

Start date
2010-06-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2010-05-21
Last updated
2014-07-14
Results posted
2014-07-14

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01128426. Inclusion in this directory is not an endorsement.