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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Trial to Assess Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Meningococcal ABCWY Vaccine as Compared to Meningococcal B Vaccine in Adolescents

ClinicalTrials.gov ID: NCT02212457

Public ClinicalTrials.gov record NCT02212457. 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 26, 2026, 12:46 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

A Phase 2b, Randomized, Controlled, Observer-Blind, Multi-Center Study Assessing the Immunogenicity and Safety of GSK Meningococcal ABCWY Vaccine Administered at Different Schedules Compared to GSK Meningococcal Group B Vaccine, in Healthy Adolescents

Study identification

NCT ID
NCT02212457
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,063 participants

Conditions and interventions

Interventions

  • Bexsero Biological
  • Saline Placebo Other
  • Havrix Biological
  • MenABCWY Biological

Biological · Other

Eligibility (public fields only)

Age range
10 Years to 18 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
Aug 20, 2014
Primary completion
May 21, 2015
Completion
Mar 2, 2016
Last update posted
Jun 26, 2019

2014 – 2016

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
GSK Investigational Site Jonesboro Arkansas 72401
GSK Investigational Site Hialeah Florida 33012
GSK Investigational Site Melbourne Florida 32934
GSK Investigational Site Augusta Kansas 67010
GSK Investigational Site Niles Michigan 49120
GSK Investigational Site Saint Paul Minnesota 55108
GSK Investigational Site Bellevue Nebraska 68005
GSK Investigational Site Omaha Nebraska 68114
GSK Investigational Site Binghamton New York 13901
GSK Investigational Site Cleveland Ohio 44122
GSK Investigational Site Dayton Ohio 45406
GSK Investigational Site Charleston South Carolina 29414
GSK Investigational Site Mt. Pleasant South Carolina 29464

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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02212457, 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 Jun 26, 2019 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02212457 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →