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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Comparison of GSKBiologicals' Hib-MenCY-TT Vaccine vs Licensed Hib Conjugate or Meningococcal Vaccine

ClinicalTrials.gov ID: NCT00129129

Public ClinicalTrials.gov record NCT00129129. 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 19, 2026, 2:39 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

Evaluate Immuno and Safety of GSKBiologicals' HibMenCYTT vs Licensed Hib Conjugate Vaccine, Each Coadministered With Pediarix® and Prevnar®, in Healthy Infants. An Exploratory Control Group Will Receive Licensed Menomune® at 3 to 5 Years

Study identification

NCT ID
NCT00129129
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
756 participants

Conditions and interventions

Interventions

  • GSK Biologicals' Haemophilus influenza type b and Neisseria meningitidis serogroups C and Y-tetanus toxoid conjugate vaccine 792014 vaccine Biological
  • ActHIB Biological
  • Pediarix Biological
  • Prevnar Biological
  • Menomune Biological

Biological

Eligibility (public fields only)

Age range
6 Weeks to 15 Months
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
Jul 31, 2004
Primary completion
Sep 14, 2005
Completion
Mar 28, 2006
Last update posted
Aug 23, 2018

2004 – 2006

United States locations

U.S. sites
27
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Fountain Valley California 92708
GSK Investigational Site Centennial Colorado 80112
GSK Investigational Site Norwich Connecticut 06360
GSK Investigational Site Marietta Georgia 30062
GSK Investigational Site Des Moines Iowa 50266
GSK Investigational Site Bardstown Kentucky 40004
GSK Investigational Site Louisville Kentucky 40202
GSK Investigational Site Louisville Kentucky 40272
GSK Investigational Site Bossier City Louisiana 71111
GSK Investigational Site Boston Massachusetts 02115
GSK Investigational Site Boston Massachusetts 02118
GSK Investigational Site New Bedford Massachusetts 02740
GSK Investigational Site Rochester New York 14620
GSK Investigational Site The Bronx New York 10467
GSK Investigational Site Boardman Ohio 44512
GSK Investigational Site University Heights Ohio 44118
GSK Investigational Site Beaver Falls Pennsylvania 15010
GSK Investigational Site Erie Pennsylvania 16505
GSK Investigational Site Greenville Pennsylvania 16125
GSK Investigational Site Norristown Pennsylvania 19401
GSK Investigational Site Pittsburgh Pennsylvania 15217
GSK Investigational Site Pittsburgh Pennsylvania 15227
GSK Investigational Site Pittsburgh Pennsylvania 15236
GSK Investigational Site Pittsburgh Pennsylvania 15241
GSK Investigational Site Rydal Pennsylvania 19046
GSK Investigational Site Warwick Rhode Island 02886

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 NCT00129129, 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 Aug 23, 2018 · Synced Jul 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00129129 live on ClinicalTrials.gov.

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