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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Immunogenicity and Safety Study of GSK's MenABCWY Vaccine in Healthy Adolescents and Adults Previously Primed With MenACWY Vaccine

ClinicalTrials.gov ID: NCT04707391

Public ClinicalTrials.gov record NCT04707391. 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, 8:41 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

A Phase IIIB, Randomized, Controlled, Observer-blind Study to Evaluate Safety and Immunogenicity of GSK's Meningococcal ABCWY Vaccine When Administered in Healthy Adolescents and Adults, Previously Primed With Meningococcal ACWY Vaccine

Brief summary

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

The purpose of this study was to assess immunogenicity and safety of MenABCWY vaccine in healthy adolescents and adults aged 15 to 25 years previously vaccinated with MenACWY vaccine.

Study identification

NCT ID
NCT04707391
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,250 participants

Conditions and interventions

Interventions

Combination Product · Biological

Eligibility (public fields only)

Age range
15 Years to 25 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
Jan 25, 2021 (Actual)
Primary completion
May 3, 2023 (Actual)
Completion
Sep 29, 2023 (Actual)
Last update posted
Jul 3, 2024

2021 – 2023

United States locations

U.S. sites
48
U.S. states
20
U.S. cities
45
Facility City State ZIP Site status
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Banning California 92220 —
GSK Investigational Site Chula Vista California 91911 —
GSK Investigational Site West Covina California 91790 —
GSK Investigational Site Washington D.C. District of Columbia 20017 —
GSK Investigational Site Miami Florida 33126 —
GSK Investigational Site Miami Florida 33135 —
GSK Investigational Site Port Orange Florida 32127 —
GSK Investigational Site Atlanta Georgia 30338 —
GSK Investigational Site Columbus Georgia 31904 —
GSK Investigational Site Sandy Springs Georgia 30328 —
GSK Investigational Site Meridian Idaho 83642 —
GSK Investigational Site Champaign Illinois 61822 —
GSK Investigational Site Quincy Illinois 62301 —
GSK Investigational Site Louisville Kentucky 40291 —
GSK Investigational Site Boston Massachusetts 02114 —
GSK Investigational Site Fall River Massachusetts 02725 —
GSK Investigational Site Methuen Massachusetts 01844 —
GSK Investigational Site Roslindale Massachusetts 02135 —
GSK Investigational Site Grosse Pointe Woods Michigan 48236 —
GSK Investigational Site Biloxi Mississippi 39531 —
GSK Investigational Site Albuquerque New Mexico 87102 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site Fayetteville North Carolina 28304 —
GSK Investigational Site Raleigh North Carolina 27612 —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Cranberry Township Pennsylvania 16066 —
GSK Investigational Site Monongahela Pennsylvania 15063 —
GSK Investigational Site Pittsburgh Pennsylvania 15025 —
GSK Investigational Site Pittsburgh Pennsylvania 15213 —
GSK Investigational Site Pittsburgh Pennsylvania 15217 —
GSK Investigational Site Warwick Rhode Island 02886-6110 —
GSK Investigational Site Charleston South Carolina 29406 —
GSK Investigational Site Greenville South Carolina 29607 —
GSK Investigational Site Austin Texas 78745 —
GSK Investigational Site Beaumont Texas 77706 —
GSK Investigational Site Carrollton Texas 75010 —
GSK Investigational Site Dallas Texas 75251 —
GSK Investigational Site Houston Texas 77055 —
GSK Investigational Site Katy Texas 77450 —
GSK Investigational Site Longview Texas 75605 —
GSK Investigational Site Plano Texas 75024 —
GSK Investigational Site The Woodlands Texas 77381-3527 —
GSK Investigational Site Kaysville Utah 84037 —
GSK Investigational Site Layton Utah 84041 —
GSK Investigational Site Roy Utah 84067 —
GSK Investigational Site Syracuse Utah 84075 —
GSK Investigational Site Seattle Washington 98105 —

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04707391, 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 Jul 3, 2024 · 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 NCT04707391 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →