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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 Jun 25, 2026, 11:34 PM 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

Study identification

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

Conditions and interventions

Interventions

  • 2-dose oral live attenuated G1P[8] human rotavirus vaccine Biological

Biological

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
May 31, 2006
Primary completion
Jan 31, 2007
Completion
May 31, 2007
Last update posted
Nov 3, 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 3, 2016 · Synced Jun 25, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00334607 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →