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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study Comparing the Immune Response and Safety of Fluarix and Fluzone Influenza Vaccines in Children

ClinicalTrials.gov ID: NCT00383123

Public ClinicalTrials.gov record NCT00383123. 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 Nov 7, 2026, 9:44 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Single-blind, Randomized Study to Evaluate the Immunogenicity and Safety of Fluarix® (GSK Biologicals') Compared With Fluzone® (Aventis Pasteur/Sanofi) Administered Intramuscularly in Children (6 Months and Older)

Brief summary

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

The purpose of this study is to compare two influenza vaccines (Fluzone and Fluarix) in terms of the immune response elicited and safety with a six month follow-up after first vaccination. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Study identification

NCT ID
NCT00383123
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
3,327 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
Nov 2, 2006 (Type not available)
Primary completion
Oct 1, 2007 (Actual)
Completion
Oct 19, 2007 (Actual)
Last update posted
Jun 8, 2018

2006 – 2007

United States locations

U.S. sites
40
U.S. states
13
U.S. cities
38
Facility City State ZIP Site status
GSK Investigational Site Antioch California 94509 —
GSK Investigational Site Fairfield California 94533 —
GSK Investigational Site Fresno California 93710 —
GSK Investigational Site Pleasanton California 94588 —
GSK Investigational Site Redwood City California 94063 —
GSK Investigational Site Richmond California 94801 —
GSK Investigational Site Rolling Hills Estates California 90274 —
GSK Investigational Site Sacramento California 95815 —
GSK Investigational Site San Francisco California 94102 —
GSK Investigational Site San Francisco California 94115 —
GSK Investigational Site Santa Clara California 95051 —
GSK Investigational Site Santa Rosa California 95403 —
GSK Investigational Site Vacaville California 95688 —
GSK Investigational Site Vallejo California 94589 —
GSK Investigational Site Walnut Creek California 94596 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site Lakewood Colorado 80401 —
GSK Investigational Site Tifton Georgia 31794 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Omaha Nebraska 68134 —
GSK Investigational Site Whitehouse Station New Jersey 08889 —
GSK Investigational Site Fishkill New York 12524 —
GSK Investigational Site Hopewell Junction New York 12533 —
GSK Investigational Site Poughkeepsie New York 12603 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site Rochester New York 14620 —
GSK Investigational Site Cary North Carolina 27518 —
GSK Investigational Site Sylva North Carolina 28779 —
GSK Investigational Site Cleveland Ohio 44118 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Uniontown Pennsylvania 15401 —
GSK Investigational Site Austin Texas 78728 —
GSK Investigational Site Fort Worth Texas 76135 —
GSK Investigational Site San Angelo Texas 76904 —
GSK Investigational Site Layton Utah 84041 —
GSK Investigational Site Salt Lake City Utah 84121 —
GSK Investigational Site South Jordan Utah 84095 —
GSK Investigational Site West Jordan Utah 84084 —

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 NCT00383123, 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 8, 2018 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00383123 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →