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Completed Phase 3 Interventional Accepts healthy volunteers Results available

A Study to Evaluate the Safety and Immunogenicity of GSK Biologicals' Seasonal Influenza Vaccine in Children

ClinicalTrials.gov ID: NCT01198756

Public ClinicalTrials.gov record NCT01198756. 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 2, 2026, 6:35 PM 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 GSK Biologicals' Quadrivalent Influenza Vaccine (GSK2282512A) When Administered in Children

Brief summary

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

This study is designed to test the immunogenicity and safety of an investigational influenza vaccine, in children compared to two other influenza vaccines.

Study identification

NCT ID
NCT01198756
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
3,109 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
6 Months to 17 Years
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
Sep 30, 2010
Primary completion
Jun 30, 2011
Completion
Jun 30, 2011
Last update posted
Sep 20, 2018

2010 – 2011

United States locations

U.S. sites
16
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
GSK Investigational Site Chandler Arizona 85224
GSK Investigational Site Scottsdale Arizona 85288
GSK Investigational Site Harrisburg Arkansas 72432
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Huntington Beach California 92647
GSK Investigational Site Paramount California 90723
GSK Investigational Site Centennial Colorado 80112
GSK Investigational Site Longmont Colorado 80501
GSK Investigational Site Thornton Colorado 80233
GSK Investigational Site Niles Michigan 49120
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Omaha Nebraska 68131
GSK Investigational Site Hermitage Pennsylvania 16148
GSK Investigational Site Barnwell South Carolina 29812
GSK Investigational Site Clarksville Tennessee 37043
GSK Investigational Site Fort Worth Texas 76135

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01198756, 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 20, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01198756 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →