Trials / Completed
CompletedNCT00452452
Study Evaluating 13-valent Pneumococcal Conjugate Vaccine Catch-Up Regimens in Older Infants and Children
A Phase 3 Open-label Trial Evaluating the Safety, Tolerability and Immunogenicity of a 13-valent Pneumococcal Conjugate Vaccine in Older Infants and Children Who Are Naive to Previous Vaccination With Pneumococcal Conjugate Vaccine.
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 355 (actual)
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer · Industry
- Sex
- All
- Age
- 7 Months – 5 Years
- Healthy volunteers
- Accepted
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 immunized with Pneumococcal vaccine.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | 13-valent Pneumococcal Conjugate Vaccine |
Timeline
- Start date
- 2007-07-01
- Primary completion
- 2008-03-01
- Completion
- 2008-03-01
- First posted
- 2007-03-27
- Last updated
- 2012-08-15
- Results posted
- 2012-08-15
Locations
9 sites across 1 country: Poland
Source: ClinicalTrials.gov record NCT00452452. Inclusion in this directory is not an endorsement.