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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immunogenicity and Safety Study of GlaxoSmithKline (GSK) Biologicals' Combined Measles-mumps-rubella (MMR) Vaccine in Subjects Four to Six Years of Age

ClinicalTrials.gov ID: NCT01621802

Public ClinicalTrials.gov record NCT01621802. 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, 1:20 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

Immunogenicity and Safety Study of GSK Biologicals' Combined Measles-mumps-rubella Vaccine in Subjects Four to Six Years of Age (209762)

Brief summary

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

The purpose of this study is to support licensure of GSK Biologicals' MMR vaccine (Priorix®) in the US by generating immunogenicity and safety data in contrast to the US standard of care, Merck's MMR vaccine (M-M-R®II), when given as a second dose to children four to six years of age.

Study identification

NCT ID
NCT01621802
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
4,011 participants

Conditions and interventions

Interventions

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
Jun 21, 2012 (Actual)
Primary completion
Jul 6, 2015 (Actual)
Completion
Nov 9, 2015 (Actual)
Last update posted
Nov 25, 2019

2012 – 2015

United States locations

U.S. sites
50
U.S. states
25
U.S. cities
47
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35205 —
GSK Investigational Site Tucson Arizona 85704 —
GSK Investigational Site Tucson Arizona 85741 —
GSK Investigational Site Benton Arkansas 72019 —
GSK Investigational Site Fayetteville Arkansas 72703 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Anaheim California 92804 —
GSK Investigational Site Baldwin Park California 91706 —
GSK Investigational Site Daly City California 94015 —
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 Sacramento California 95815 —
GSK Investigational Site Sacramento California 95823 —
GSK Investigational Site Santa Clara California 95051 —
GSK Investigational Site Walnut Creek California 94596 —
GSK Investigational Site Colorado Springs Colorado 80922 —
GSK Investigational Site Altamonte Springs Florida 32701 —
GSK Investigational Site Marietta Georgia 30062 —
GSK Investigational Site Woodstock Georgia 30189 —
GSK Investigational Site Nampa Idaho 83686 —
GSK Investigational Site Indianapolis Indiana 46256 —
GSK Investigational Site Augusta Kansas 67010 —
GSK Investigational Site Newton Kansas 67114 —
GSK Investigational Site Bardstown Kentucky 40004 —
GSK Investigational Site Columbia Maryland 21045 —
GSK Investigational Site Fall River Massachusetts 02721 —
GSK Investigational Site The Bronx New York 10467 —
GSK Investigational Site Asheboro North Carolina 27203 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Cincinnati Ohio 45245 —
GSK Investigational Site Cleveland Ohio 44121 —
GSK Investigational Site Dayton Ohio 45406 —
GSK Investigational Site Dayton Ohio 45414 —
GSK Investigational Site Gresham Oregon 97030 —
GSK Investigational Site Erie Pennsylvania 16505 —
GSK Investigational Site Charleston South Carolina 29414 —
GSK Investigational Site Cheraw South Carolina 29520 —
GSK Investigational Site Rapid City South Dakota 57701 —
GSK Investigational Site Houston Texas 77055 —
GSK Investigational Site Tomball Texas 77375 —
GSK Investigational Site Provo Utah 84604 —
GSK Investigational Site Salt Lake City Utah 84109 —
GSK Investigational Site South Jordan Utah 84095 —
GSK Investigational Site St. George Utah 84790 —
GSK Investigational Site Burke Virginia 22015 —
GSK Investigational Site Charlottesville Virginia 22902 —
GSK Investigational Site Huntington West Virginia 25701 —
GSK Investigational Site Monroe Wisconsin 53566 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01621802, 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 25, 2019 · 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 NCT01621802 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →