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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immunogenicity and Safety Study of GSK Biologicals' Influenza Vaccine When Administered in Children

ClinicalTrials.gov ID: NCT01196988

Public ClinicalTrials.gov record NCT01196988. 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 31, 2026, 5:28 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' Influenza Vaccine GSK2321138A When Administered in Children

Brief summary

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

This study is designed to assess the safety and immunogenicity of GlaxoSmithKline (GSK) Biologicals' investigational vaccine GSK2321138A in children aged 3 to 17 years, and to describe safety and immunogenicity of the GSK Biologicals' investigational vaccine GSK2321138A in children aged 6 to 35 months.

Study identification

NCT ID
NCT01196988
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
3,027 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
Oct 4, 2010 (Type not available)
Primary completion
Jun 15, 2011 (Actual)
Completion
Jun 15, 2011 (Actual)
Last update posted
Sep 21, 2018

2010 – 2011

United States locations

U.S. sites
14
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
GSK Investigational Site Sacramento California 95816 —
GSK Investigational Site Boca Raton Florida 33432 —
GSK Investigational Site Wichita Kansas 67205 —
GSK Investigational Site Wichita Kansas 67207 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Boston Massachusetts 02130 —
GSK Investigational Site Omaha Nebraska 68134 —
GSK Investigational Site Binghamton New York 13901 —
GSK Investigational Site Elmira New York 14901 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Houston Texas 77055 —
GSK Investigational Site San Angelo Texas 76904 —

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 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01196988, 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 21, 2018 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01196988 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →