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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Immunogenicity and Safety of Meningococcal Vaccine GSK134612 Given as 1 or 2 Doses to Healthy 9-12 Months Old Toddlers.

ClinicalTrials.gov ID: NCT00471081

Public ClinicalTrials.gov record NCT00471081. 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 Sep 3, 2026, 1:03 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

Study to Assess Immunogenicity, Reactogenicity and Safety of Primary Vaccination With GSK Biologicals' MenACWY Vaccine (GSK134612) Given as 1 or 2 Doses to Healthy Toddlers 9-12 Months of Age

Brief summary

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

The purpose of the study is to characterize the safety and immunogenicity of 1 dose of GSK134612 vaccine at 12 months of age and of GSK134612 vaccine administered as 2 doses at 9 and 12 months of age.

Study identification

NCT ID
NCT00471081
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
385 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
9 Months to 9 Months
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
Jul 4, 2007
Primary completion
Oct 22, 2008
Completion
Nov 25, 2008
Last update posted
Jun 24, 2019

2007 – 2008

United States locations

U.S. sites
19
U.S. states
8
U.S. cities
18
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35205
GSK Investigational Site Benton Arkansas 72015
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Antioch California 94509
GSK Investigational Site Fremont California 94538
GSK Investigational Site Hayward California 94545
GSK Investigational Site Madera California 93637
GSK Investigational Site Santa Rosa California 95403
GSK Investigational Site Vacaville California 95688
GSK Investigational Site Lakewood Colorado 80226
GSK Investigational Site Littleton Colorado 80122
GSK Investigational Site Littleton Colorado 80234
GSK Investigational Site Westminster Colorado 80234
GSK Investigational Site Wheat Ridge Colorado 80033
GSK Investigational Site Birmingham Georgia 35244
GSK Investigational Site Canton Ohio 44718
GSK Investigational Site Erie Pennsylvania 16501
GSK Investigational Site Greenville Pennsylvania 16125
GSK Investigational Site Amarillo Texas 79124

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 NCT00471081, 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 Jun 24, 2019 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00471081 live on ClinicalTrials.gov.

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