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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immune Response and Safety Comparison of 3 Lots of GSK Biologicals' DTaP-IPV Candidate Vaccine to DTaP + IPV Vaccines

ClinicalTrials.gov ID: NCT00148941

Public ClinicalTrials.gov record NCT00148941. 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, 6:50 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

Safety, Immunogenicity and Consistency of 3 Manufacturing Lots of DTaP-IPV Vaccine Versus Separate Injections of GSK Biologicals' DTaP + Aventis Pasteur's IPV Administered as Booster Doses to Healthy Children 4-6 Years, Each Co-administered With Merck's MMR Vaccine

Study identification

NCT ID
NCT00148941
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
4,209 participants

Conditions and interventions

Interventions

  • SB213503 lot 1 Biological
  • SB213503 lot 2 Biological
  • SB213503 lot 3 Biological
  • Infanrix Biological
  • IPOL Biological
  • M-M-R II Biological

Biological

Eligibility (public fields only)

Age range
4 Years to 6 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 5, 2005
Primary completion
Oct 31, 2006
Completion
Dec 3, 2006
Last update posted
Feb 4, 2020

2005 – 2006

United States locations

U.S. sites
24
U.S. states
4
U.S. cities
23
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Antioch California 94509
GSK Investigational Site Daly City California 94015
GSK Investigational Site Fairfield California 94533
GSK Investigational Site Fremont California 94538
GSK Investigational Site Fresno California 93726
GSK Investigational Site Hayward California 94545
GSK Investigational Site Oakland California 94611
GSK Investigational Site Pleasanton California 94588
GSK Investigational Site Redwood City California 94063
GSK Investigational Site Richmond California 94801
GSK Investigational Site Roseville California 95661
GSK Investigational Site Sacramento California 95823
GSK Investigational Site Sacramento California 95825
GSK Investigational Site San Francisco California 94115
GSK Investigational Site San Jose California 95119
GSK Investigational Site San Ramon California 94583
GSK Investigational Site Santa Clara California 95051
GSK Investigational Site Santa Rosa California 95403
GSK Investigational Site Vacaville California 95688
GSK Investigational Site Vallejo California 94589
GSK Investigational Site Walnut Creek California 94596
GSK Investigational Site Columbus Ohio 43214
GSK Investigational Site Mechanicsville Virginia 23111

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 NCT00148941, 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 Feb 4, 2020 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00148941 live on ClinicalTrials.gov.

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