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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 Children in Their Second Year of Life

ClinicalTrials.gov ID: NCT01681992

Public ClinicalTrials.gov record NCT01681992. 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, 6:49 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

Immunogenicity and Safety Study of GSK Biologicals' Priorix Vaccine (209762) at an End of Shelf-life Potency Compared to Merck & Co., Inc.'s Measles-mumps-rubella (MMR) Vaccine When Both Are Given on a 2-dose Schedule to Healthy Children in Their 2nd Year of Life

Study identification

NCT ID
NCT01681992
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
4,538 participants

Conditions and interventions

Interventions

  • Priorix Biological
  • M-M-R II Biological
  • Varivax Biological
  • Havrix Biological
  • Prevnar 13 Biological

Biological

Eligibility (public fields only)

Age range
12 Months 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
Oct 9, 2012
Primary completion
Feb 2, 2015
Completion
Aug 17, 2015
Last update posted
Jan 6, 2021

2012 – 2015

United States locations

U.S. sites
40
U.S. states
21
U.S. cities
36
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35205
GSK Investigational Site Phoenix Arizona 85012
GSK Investigational Site Phoenix Arizona 85032
GSK Investigational Site Jonesboro Arkansas 72401
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site West Covina California 91790
GSK Investigational Site Altamonte Springs Florida 32701
GSK Investigational Site Miami Florida 33184
GSK Investigational Site Miami Lakes Florida 33014
GSK Investigational Site Naples Florida 34102
GSK Investigational Site Tampa Florida 33606
GSK Investigational Site Muncie Indiana 47304-5547
GSK Investigational Site New Albany Indiana 47150
GSK Investigational Site West Des Moines Iowa 50265
GSK Investigational Site Wichita Kansas 67205
GSK Investigational Site Louisville Kentucky 40207
GSK Investigational Site Annapolis Maryland 21401
GSK Investigational Site Baltimore Maryland 21201
GSK Investigational Site Frederick Maryland 21702
GSK Investigational Site Kansas City Missouri 64108
GSK Investigational Site Lincoln Nebraska 68504
GSK Investigational Site Lincoln Nebraska 68505
GSK Investigational Site Omaha Nebraska 68131
GSK Investigational Site Clyde North Carolina 28721
GSK Investigational Site Cleveland Ohio 44121
GSK Investigational Site Dayton Ohio 45406
GSK Investigational Site Dayton Ohio 45414
GSK Investigational Site Toledo Ohio 43606
GSK Investigational Site Youngstown Ohio 44514
GSK Investigational Site Gresham Oregon 97030
GSK Investigational Site Johnstown Pennsylvania 15904
GSK Investigational Site Charleston South Carolina 29406
GSK Investigational Site Charleston South Carolina 29414
GSK Investigational Site Houston Texas 77087
GSK Investigational Site Layton Utah 84041
GSK Investigational Site Springville Utah 84663
GSK Investigational Site St. George Utah 84790
GSK Investigational Site Midlothian Virginia 23113
GSK Investigational Site Richmond Virginia 23223
GSK Investigational Site Ellensburg Washington 98926

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 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01681992, 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 Jan 6, 2021 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01681992 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →