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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Safety and Immunogenicity of H1N1 Vaccines in Children Aged 6 Months to Less Than 9 Years of Age

ClinicalTrials.gov ID: NCT00976820

Public ClinicalTrials.gov record NCT00976820. 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 Oct 19, 2026, 4:25 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

A Study to Evaluate the Safety and Immunogenicity of A/California/7/2009 (H1N1)V-like Vaccines GSK2340274A and GSK2340273A in Children 6 Months to Less Than 9 Years of Age

Brief summary

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

The purpose of this study is to characterize the safety and immune response of the H1N1 (swine) flu vaccines GSK2340274A and GSK2340273A in children 6 months to less than 9 years of age. This Protocol Posting has been updated following the Protocol amendment 1 \& 2, September and October 2009. The sections impacted are study design, objectives and analysis methods.

Study identification

NCT ID
NCT00976820
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
323 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
6 Months to 8 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
Oct 20, 2009 (Actual)
Primary completion
Mar 21, 2011 (Actual)
Completion
Mar 21, 2011 (Actual)
Last update posted
Dec 12, 2017

2009 – 2011

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
GSK Investigational Site Conway Arkansas 72034 —
GSK Investigational Site Little Rock Arkansas 72202 —
GSK Investigational Site Sacramento California 95816 —
GSK Investigational Site San Francisco California 94102 —
GSK Investigational Site Arkansas City Kansas 67005 —
GSK Investigational Site Wichita Kansas 67205 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Saint Paul Minnesota 55108 —
GSK Investigational Site Omaha Nebraska 68134 —
GSK Investigational Site Cleveland Ohio 44121 —
GSK Investigational Site Kingsport Tennessee 37660 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Fort Worth Texas 76135 —
GSK Investigational Site San Angelo Texas 76904 —
GSK Investigational Site Orem Utah 84057 —
GSK Investigational Site South Jordan Utah 84095 —

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 NCT00976820, 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 Dec 12, 2017 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00976820 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →