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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Safety, Immunogenicity, and Relative Efficacy of H1N1 Vaccines in Adults Aged 18 Years and Older

ClinicalTrials.gov ID: NCT00979602

Public ClinicalTrials.gov record NCT00979602. 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 4, 2026, 7:31 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

A Study to Evaluate the Safety, Immunogenicity, and Relative Efficacy of A/California/7/2009 (H1N1)V-like Vaccines GSK2340274A and GSK2340273A in Adults Aged 18 Years and Older

Brief summary

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

The purpose of this study is to characterize the safety, immunogenicity, and relative efficacy of the H1N1 (swine) flu vaccines GSK2340273A and GSK2340274A in adults 18 years of age or older.

Study identification

NCT ID
NCT00979602
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
4,048 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years and older
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 8, 2009
Primary completion
Jan 9, 2011
Completion
Jan 31, 2011
Last update posted
Mar 20, 2018

2009 – 2011

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
24
Facility City State ZIP Site status
GSK Investigational Site Mesa Arizona 85213
GSK Investigational Site Phoenix Arizona 85020
GSK Investigational Site Phoenix Arizona 85028
GSK Investigational Site Los Angeles California 90057
GSK Investigational Site Clearwater Florida 33761
GSK Investigational Site DeLand Florida 32720
GSK Investigational Site Delray Beach Florida 33484
GSK Investigational Site Jacksonville Florida 32205
GSK Investigational Site Chicago Illinois 60610
GSK Investigational Site Wichita Kansas 67207
GSK Investigational Site Lexington Kentucky 40509
GSK Investigational Site Columbia Maryland 21045
GSK Investigational Site Rockville Maryland 20850
GSK Investigational Site Milford Massachusetts 01757
GSK Investigational Site Kansas City Missouri 64114
GSK Investigational Site Somers Point New Jersey 08244
GSK Investigational Site Binghamton New York 13901
GSK Investigational Site Camillus New York 13031
GSK Investigational Site Winston-Salem North Carolina 27103
GSK Investigational Site Willoughby Hills Ohio 44094
GSK Investigational Site Erie Pennsylvania 16506
GSK Investigational Site Warwick Rhode Island 02886
GSK Investigational Site Spartanburg South Carolina 29303
GSK Investigational Site Nashville Tennessee 37203
GSK Investigational Site Wenatchee Washington 98801

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 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00979602, 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 Mar 20, 2018 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00979602 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →