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Completed Phase 3 Interventional Accepts healthy volunteers Results available

Study to Evaluate the Immune Response After a Booster Dose of a Quadrivalent Meningococcal (MenACYW) Conjugate Vaccine When Administered Alone or Concomitantly With a Licensed Meningococcal Serogroup B Vaccine, in Participants Who Received Primary Quadrivalent Meningococcal Conjugate Vaccine (MCV4)

ClinicalTrials.gov ID: NCT04084769

Public ClinicalTrials.gov record NCT04084769. 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 24, 2026, 2:40 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 of a Booster Dose of an Investigational Quadrivalent Meningococcal Conjugate Vaccine in Adolescents and Adults

Study identification

NCT ID
NCT04084769
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi Pasteur, a Sanofi Company
Industry
Enrollment
570 participants

Conditions and interventions

Interventions

  • Meningococcal polysaccharide (serogroups A, C, Y, and W) tetanus toxoid Conjugate vaccine MenACYW Conjugate vaccine Biological
  • Meningococcal Group B vaccine (Trumenba®) Biological
  • Meningococcal group B vaccine (Bexsero®) Biological

Biological

Eligibility (public fields only)

Age range
13 Years to 26 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
Sep 2, 2019
Primary completion
Sep 13, 2020
Completion
Sep 13, 2020
Last update posted
Sep 14, 2025

2019 – 2020

United States locations

U.S. sites
29
U.S. states
12
U.S. cities
23
Facility City State ZIP Site status
Investigational Site Number 8400012 Birmingham Alabama 35205
Investigational Site Number 8400005 San Diego California 92123-1881
Investigational Site Number 8400013 Bardstown Kentucky 40004
Investigational Site Number 8400033 Lexington Kentucky 40517
Investigational Site Number 8400034 Bridgeton Missouri 63044
Investigational Site Number 8400027 Lincoln Nebraska 68504
Investigational Site Number 8400002 Lincoln Nebraska 68505
Investigational Site Number 8400004 Lincoln Nebraska 68516
Investigational Site Number 8400030 Dayton Ohio 45414
Investigational Site Number 8400028 South Euclid Ohio 44121
Investigational Site Number 8400009 Norman Oklahoma 73069
Investigational Site Number 8400038 Erie Pennsylvania 16505
Investigational Site Number 8400039 Charleston South Carolina 29414
Investigational Site Number 8400018 Kingsport Tennessee 37660
Investigational Site Number 8400029 Tullahoma Tennessee 37388
Investigational Site Number 8400031 Kaysville Utah 84037
Investigational Site Number 8400001 Layton Utah 84041
Investigational Site Number 8400014 Layton Utah 84041
Investigational Site Number 8400040 Orem Utah 84057
Investigational Site Number 8400011 Provo Utah 84064
Investigational Site Number 8400023 Roy Utah 84067
Investigational Site Number 8400003 Salt Lake City Utah 84107
Investigational Site Number 8400007 Salt Lake City Utah 84109
Investigational Site Number 8400022 Salt Lake City Utah 84109
Investigational Site Number 8400015 South Jordan Utah 84095
Investigational Site Number 8400036 South Jordan Utah 84095
Investigational Site Number 8400032 Syracuse Utah 84075-9645
Investigational Site Number 8400024 West Jordan Utah 84088-8865
Investigational Site Number 8400037 Charlottesville Virginia 22903

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04084769, 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 Sep 14, 2025 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04084769 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →