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Completed Phase 3 Interventional Accepts healthy volunteers

Study of 2 Doses of HRV Vaccine Given Concomitantly or Separately With Routine Vaccinations in Healthy Infants in USA

ClinicalTrials.gov ID: NCT00334607

Public ClinicalTrials.gov record NCT00334607. 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 17, 2026, 11:02 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

Assess the Immunogenicity of 3 Doses of Pediarix®, Prevnar® & ActHIB® Given to Healthy Infants When Administered With GSK Biologicals' 2 Dose Oral Live Attenuated Human Rotavirus Vaccine Given During the Same Vaccination Visit or Separately

Brief summary

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

The aim of this this study is to confirm absence of immune interference between HRV vaccine and routine infant vaccinations currently in use in the USA.

Study identification

NCT ID
NCT00334607
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
484 participants

Conditions and interventions

Eligibility (public fields only)

Age range
6 Weeks to 16 Weeks
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
Jun 2006 (Type not available)
Primary completion
Feb 2007 (Actual)
Completion
Jun 2007 (Actual)
Last update posted
Nov 4, 2016

2006 – 2007

United States locations

U.S. sites
42
U.S. states
17
U.S. cities
40
Facility City State ZIP Site status
GSK Investigational Site Benton Arkansas 72015 —
GSK Investigational Site Cabot Arkansas 72023 —
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site North Little Rock Arkansas 72117 —
GSK Investigational Site Lakewood California 90711 —
GSK Investigational Site Paramount California 90723 —
GSK Investigational Site Pasadena California 91107 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site DeKalb Illinois 60115 —
GSK Investigational Site Overland Park Kansas 66202 —
GSK Investigational Site Commerce Twp Michigan 48382 —
GSK Investigational Site Lebanon New Hampshire 03756 —
GSK Investigational Site Bryson City North Carolina 28713 —
GSK Investigational Site Clyde North Carolina 28721 —
GSK Investigational Site Deerfield North Carolina 28607 —
GSK Investigational Site Franklin North Carolina 28734 —
GSK Investigational Site Laurinburg North Carolina 28352 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Akron Ohio 44304 —
GSK Investigational Site Boardman Ohio 44512 —
GSK Investigational Site Dayton Ohio 45406 —
GSK Investigational Site Youngstown Ohio 44505 —
GSK Investigational Site Youngstown Ohio 44514 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site East Providence Rhode Island 02914 —
GSK Investigational Site Providence Rhode Island 02903 —
GSK Investigational Site Charleston South Carolina 29407 —
GSK Investigational Site Charleston South Carolina 29412 —
GSK Investigational Site North Charleston South Carolina 29405 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Kingsport Tennessee 37660 —
GSK Investigational Site Bryan Texas 77802 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site Layton Utah 84041 —
GSK Investigational Site Ogden Utah 84405 —
GSK Investigational Site Orem Utah 84057 —
GSK Investigational Site Provo Utah 84604 —
GSK Investigational Site South Jordan Utah 84095 —
GSK Investigational Site West Jordan Utah 84088 —
GSK Investigational Site Charlottesville Virginia 22911 —
GSK Investigational Site Marshfield Wisconsin 54449 —

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 NCT00334607, 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 Nov 4, 2016 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00334607 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →