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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Boostrix™ Vaccine in Previously Boosted Young Adults

ClinicalTrials.gov ID: NCT01738477

Public ClinicalTrials.gov record NCT01738477. 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 20, 2026, 4:51 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 Immunogenicity and Safety of GSK Biologicals' Tdap Booster Vaccine (Boostrix™) in Young Adults, Administered 10 Years After Previous Tdap Boosting

Brief summary

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

The purpose of this follow-up study is to evaluate the persistence of antibodies against all the vaccine antigens 10 years after booster vaccination with either Tdap or Td, and also to assess immunogenicity and safety of another dose of Boostrix, administered in this study. This protocol posting deals with objectives and outcome measures of the extension phase. The objectives and outcome measures of the primary phase are presented in a separate protocol posting (NCT number = NCT00109330).

Study identification

NCT ID
NCT01738477
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
165 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
19 Years to 30 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
Jan 31, 2013 (Actual)
Primary completion
Apr 2, 2014 (Actual)
Completion
Apr 2, 2014 (Actual)
Last update posted
Jun 6, 2018

2013 – 2014

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site Mesa Arizona 85213 —
GSK Investigational Site Tempe Arizona 85283 —
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Rolling Hills Estates California 90274 —
GSK Investigational Site Golden Colorado 80401 —
GSK Investigational Site Norwich Connecticut 06360 —
GSK Investigational Site Jacksonville Florida 32209 —
GSK Investigational Site Chicago Illinois 60614 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Woburn Massachusetts 01801 —
GSK Investigational Site Omaha Nebraska 68131 —
GSK Investigational Site East Setauket New York 11733 —
GSK Investigational Site Cleveland Ohio 44109 —
GSK Investigational Site Cleveland Ohio 44121 —
GSK Investigational Site Erie Pennsylvania 16505 —
GSK Investigational Site Upper Saint Clair Pennsylvania 15241 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Salt Lake City Utah 84109 —
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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01738477, 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 6, 2018 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01738477 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →