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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study to Evaluate the Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Quadrivalent Influenza Vaccine (GSK2282512A) Compared to Fluzone® Quadrivalent in Children 6 to 35 Months of Age

ClinicalTrials.gov ID: NCT02242643

Public ClinicalTrials.gov record NCT02242643. 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, 10:12 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 GSK Biologicals' Quadrivalent Influenza Vaccine (GSK2282512A) Compared to Fluzone® Quadrivalent in Children 6 to 35 Months of Age

Brief summary

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

The purpose of this study is to assess the immunogenicity and safety of GSK Biologicals' quadrivalent influenza vaccine (GSK2282512A) compared to Sanofi Pasteur's Fluzone® Quadrivalent in children 6 to 35 months of age.

Study identification

NCT ID
NCT02242643
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
2,432 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
6 Months to 35 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
Sep 30, 2014
Primary completion
Mar 15, 2015
Completion
Jun 22, 2015
Last update posted
Sep 6, 2018

2014 – 2015

United States locations

U.S. sites
64
U.S. states
26
U.S. cities
59
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35235
GSK Investigational Site Dothan Alabama 36305
GSK Investigational Site Tucson Arizona 85741
GSK Investigational Site Jonesboro Arkansas 72401
GSK Investigational Site Anaheim California 92804
GSK Investigational Site Chino California 91710
GSK Investigational Site Daly City California 94015
GSK Investigational Site Fresno California 93726
GSK Investigational Site Hayward California 94545
GSK Investigational Site Oakland California 94611
GSK Investigational Site Paramount California 90723
GSK Investigational Site Pleasanton California 94588
GSK Investigational Site Sacramento California 95815
GSK Investigational Site Sacramento California 95822
GSK Investigational Site Sacramento California 95823
GSK Investigational Site Santa Clara California 95051
GSK Investigational Site Walnut Creek California 94596
GSK Investigational Site West Covina California 91790
GSK Investigational Site Colorado Springs Colorado 80920
GSK Investigational Site Colorado Springs Colorado 80922
GSK Investigational Site Lake Mary Florida 32736
GSK Investigational Site Miami Lakes Florida 33014
GSK Investigational Site Nampa Idaho 83686
GSK Investigational Site Augusta Kansas 67010
GSK Investigational Site Newton Kansas 67114
GSK Investigational Site Topeka Kansas 66604
GSK Investigational Site Wichita Kansas 67207
GSK Investigational Site Louisville Kentucky 40291
GSK Investigational Site Bossier City Louisiana 71111
GSK Investigational Site Metairie Louisiana 70006
GSK Investigational Site Columbia Maryland 21045
GSK Investigational Site Woburn Massachusetts 01801
GSK Investigational Site St Louis Missouri 63141
GSK Investigational Site Lincoln Nebraska 68504
GSK Investigational Site Lincoln Nebraska 68505
GSK Investigational Site Lincoln Nebraska 68516
GSK Investigational Site Las Vegas Nevada 89104
GSK Investigational Site Binghamton New York 13901
GSK Investigational Site Syracuse New York 13210
GSK Investigational Site Raleigh North Carolina 27609
GSK Investigational Site Beavercreek Ohio 45431
GSK Investigational Site Cleveland Ohio 44121
GSK Investigational Site Dayton Ohio 45406
GSK Investigational Site Erie Pennsylvania 16505
GSK Investigational Site Hermitage Pennsylvania 16148
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Sellersville Pennsylvania 18960
GSK Investigational Site Charleston South Carolina 29406
GSK Investigational Site Cheraw South Carolina 29520
GSK Investigational Site Kingsport Tennessee 37660
GSK Investigational Site Austin Texas 78705
GSK Investigational Site Fort Worth Texas 76135
GSK Investigational Site Galveston Texas 77555-1119
GSK Investigational Site Tomball Texas 77375
GSK Investigational Site Layton Utah 84041
GSK Investigational Site Orem Utah 84057
GSK Investigational Site Payson Utah 84651
GSK Investigational Site Provo Utah 84604
GSK Investigational Site Roy Utah 84067
GSK Investigational Site Salt Lake City Utah 84124
GSK Investigational Site South Jordan Utah 84095
GSK Investigational Site Charlottesville Virginia 22902
GSK Investigational Site Ellensburg Washington 98926
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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02242643, 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 6, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02242643 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →