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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immunogenicity, Safety of GSKs Tdap Vaccine Boostrix When Coadministered With GSKs Influenza Vaccine Fluarix in Adults

ClinicalTrials.gov ID: NCT00385255

Public ClinicalTrials.gov record NCT00385255. 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 Jul 21, 2026, 10:59 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 Immunogenicity and Safety of Boostrix When Co-administered With Fluarix in Subjects 19 Years of Age and Older

Study identification

NCT ID
NCT00385255
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,726 participants

Conditions and interventions

Interventions

  • Fluarix® Biological
  • Boostrix® Biological

Biological

Eligibility (public fields only)

Age range
19 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
Oct 22, 2006
Primary completion
Feb 27, 2007
Completion
Feb 27, 2007
Last update posted
Jun 9, 2019

2006 – 2007

United States locations

U.S. sites
12
U.S. states
7
U.S. cities
11
Facility City State ZIP Site status
GSK Investigational Site Huntsville Alabama 35802
GSK Investigational Site Chandler Arizona 85224
GSK Investigational Site Mesa Arizona 85213
GSK Investigational Site Phoenix Arizona 85014
GSK Investigational Site Inverness Florida 34452
GSK Investigational Site Melbourne Florida 32935
GSK Investigational Site Pembroke Pines Florida 33024
GSK Investigational Site Peoria Illinois 61602
GSK Investigational Site Pittsburgh Pennsylvania 15217
GSK Investigational Site Pittsburgh Pennsylvania 15220
GSK Investigational Site Bristol Tennessee 37620
GSK Investigational Site Houston Texas 77024

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 NCT00385255, 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 9, 2019 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00385255 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →