CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 354 enrolled
Drug / intervention
13-Valent Pneumococcal Conjugate Vaccine (13vPnC) +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00676091
NCT00676091Phase 3Completed

A Phase 3, Randomized, Active-Controlled, Double-Blind Trial Evaluating the Safety, Tolerability, and Immunogenicity of a 13-valent Pneumococcal Conjugate Vaccine in Healthy Infants Given With Routine Pediatric Vaccinations in Brazil

Wyeth is now a wholly owned subsidiary of Pfizer·interventional·Posted May 12, 2008·Updated Aug 8, 2011

In Brief

A Phase 3 clinical trial evaluating 13-Valent Pneumococcal Conjugate Vaccine (13vPnC) and 7-Valent Pneumococcal Conjugate Vaccine (7vPnc) for Vaccines, Pneumococcal Conjugate Vaccine. Completed, enrolled 354 participants across 4 sites.

Detailed Summary

The purpose of this study will be to analyze 13-valent pneumococcal vaccine given to healthy infants in Brazil for safety and tolerability, and to determine the immune response to the vaccines.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBrazil
Collaborators--

Timeline

Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMay 12, 2008
Enrollment StartApr 1, 2008
Primary CompletionSep 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 18.1 years ago

Interventions

13-Valent Pneumococcal Conjugate Vaccine (13vPnC)biological

7-Valent Pneumococcal Conjugate Vaccine (7vPnc)biological