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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immuno,Safety of GSK Vaccine 134612 Given at Age of 12-15 Months 15-18 Months Post-priming With GSK Vaccine 792014

ClinicalTrials.gov ID: NCT00614614

Public ClinicalTrials.gov record NCT00614614. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 3:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Immunogenicity and Safety Study of a Booster Dose of GSK Biologicals' Meningococcal Vaccine 134612 Given at 12-15 Months of Age or at 15-18 Months of Age (Co-administered With Infanrix®) in Primed Healthy Toddlers.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to characterize the immunogenicity \& safety of a booster dose of GSK Biologicals' meningococcal vaccine 134612 given at 12-15 months of age or at 15-18 months of age (co-administered with Infanrix®) in healthy toddlers primed with GSK Biological's Hib-meningococcal vaccine 792014. This study is single-blinded for the primary phase and open-label for the booster phase.

Study identification

NCT ID
NCT00614614
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,558 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Weeks to 12 Weeks
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 13, 2008 (Type not available)
Primary completion
Jul 31, 2009 (Actual)
Completion
Sep 17, 2009 (Actual)
Last update posted
Sep 21, 2018

2008 – 2009

United States locations

U.S. sites
56
U.S. states
23
U.S. cities
53
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35205 —
GSK Investigational Site Birmingham Alabama 35244 —
GSK Investigational Site Dothan Alabama 36305 —
GSK Investigational Site Benton Arkansas 72019 —
GSK Investigational Site Fayetteville Arkansas 72703 —
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Fresno California 93726 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site West Covina California 91790 —
GSK Investigational Site Plantation Florida 33324 —
GSK Investigational Site West Palm Beach Florida 33407 —
GSK Investigational Site Marietta Georgia 30062 —
GSK Investigational Site Woodstock Georgia 30189 —
GSK Investigational Site Nampa Idaho 208 463 3126 —
GSK Investigational Site Des Moines Iowa 50312 —
GSK Investigational Site West Des Moines Iowa 50266 —
GSK Investigational Site Arkansas City Kansas 67005 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Lexington Kentucky 40503 —
GSK Investigational Site Bossier City Louisiana 71111 —
GSK Investigational Site Boston Massachusetts 02130 —
GSK Investigational Site Fall River Massachusetts 02724 —
GSK Investigational Site Kalamazoo Michigan 49008 —
GSK Investigational Site Niles Michigan 49120 —
GSK Investigational Site Portage Michigan 49024 —
GSK Investigational Site Richland Michigan 49083 —
GSK Investigational Site Stevensville Michigan 49127 —
GSK Investigational Site Saint Paul Minnesota 55108 —
GSK Investigational Site Henderson Nevada 89015 —
GSK Investigational Site Clyde North Carolina 28721 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Cleveland Ohio 44121 —
GSK Investigational Site Huber Heights Ohio 45424 —
GSK Investigational Site Gresham Oregon 97030 —
GSK Investigational Site Erie Pennsylvania 16505 —
GSK Investigational Site Greenville Pennsylvania 16125 —
GSK Investigational Site Pittsburgh Pennsylvania 15220 —
GSK Investigational Site Pittsburgh Pennsylvania 15236 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Uniontown Pennsylvania 15401 —
GSK Investigational Site Charleston South Carolina 29406 —
GSK Investigational Site Kingsport Tennessee 37660 —
GSK Investigational Site Amarillo Texas 79124 —
GSK Investigational Site Galveston Texas 77555-1119 —
GSK Investigational Site Sugar Land Texas 77479 —
GSK Investigational Site Layton Utah 84041 —
GSK Investigational Site Ogden Utah 84405 —
GSK Investigational Site Orem Utah 84057 —
GSK Investigational Site Provo Utah 84604 —
GSK Investigational Site Roy Utah 84067 —
GSK Investigational Site South Jordan Utah 84095 —
GSK Investigational Site St. George Utah 84790 —
GSK Investigational Site Syracuse Utah 84075 —
GSK Investigational Site Marshfield Wisconsin 54449 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00614614, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 21, 2018 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00614614 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →