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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Evaluation of GlaxoSmithKline Biologicals' Boostrix® Vaccine in Comparison With Decavac™ Vaccine.

ClinicalTrials.gov ID: NCT00835237

Public ClinicalTrials.gov record NCT00835237. 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 21, 2026, 3:45 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

Evaluation of GSK Biologicals' Boostrix® Vaccine When Compared With Decavac™ in Adults Aged 65 Years or Older.

Brief summary

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

This phase IIIb, observer-blind study will evaluate the immunogenicity and safety of GSK Biologicals' Boostrix® vaccine in adults (extending indication) aged 65 years or older.

Study identification

NCT ID
NCT00835237
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,332 participants

Conditions and interventions

Eligibility (public fields only)

Age range
65 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
Feb 17, 2009 (Actual)
Primary completion
Jul 23, 2009 (Actual)
Completion
Oct 15, 2009 (Actual)
Last update posted
Jan 3, 2020

2009

United States locations

U.S. sites
24
U.S. states
19
U.S. cities
24
Facility City State ZIP Site status
GSK Investigational Site Tucson Arizona 85741 —
GSK Investigational Site Los Angeles California 90057 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site West Palm Beach Florida 33409 —
GSK Investigational Site Stockbridge Georgia 30281 —
GSK Investigational Site Indianapolis Indiana 46254 —
GSK Investigational Site Pratt Kansas 67124 —
GSK Investigational Site Lexington Kentucky 40509 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Columbia Maryland 21045 —
GSK Investigational Site Elkridge Maryland 21075 —
GSK Investigational Site Milford Massachusetts 01757 —
GSK Investigational Site Stevensville Michigan 49127 —
GSK Investigational Site High Point North Carolina 27262 —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Cleveland Ohio 44122 —
GSK Investigational Site Mogadore Ohio 44260 —
GSK Investigational Site Wadsworth Ohio 44281 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Fort Worth Texas 76135 —
GSK Investigational Site West Jordan Utah 84088 —
GSK Investigational Site Williamsburg Virginia 23185 —
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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00835237, 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 Jan 3, 2020 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00835237 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →