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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 Oct 24, 2026, 1:37 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 of a Booster Dose of an Investigational Quadrivalent Meningococcal Conjugate Vaccine in Adolescents and Adults

Brief summary

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

Primary Objective: To demonstrate the vaccine seroresponse sufficiency of meningococcal serogroups A, C, Y, and W following the administration of a booster dose of meningococcal Polysaccharide (Serogroups A, C, Y and W) Tetanus Toxoid (MenACYW) Conjugate vaccine: * In Group 1 participants who were first vaccinated with 1 dose of MenACYW Conjugate vaccine 3-6 years before the booster dose. * In Group 2 participants who were first vaccinated with 1 dose of Menveo vaccine (meningococcal \[Groups A, C, Y and W135\] Oligosaccharide Diphtheria CRM197 Conjugate vaccine) 3-6 years before the booster dose. Secondary Objective: To describe: * The vaccine seroresponse, seroprotection (serum bactericidal assay using human complement \[hSBA\] titer greater than or equal to \[\>=\]1:8), and antibody responses (geometric mean titers \[GMTs\]) of meningococcal serogroups A, C, Y, and W measured using hSBA in serum specimens collected 6 days (±1 day) after vaccination in a subset of 50 participants per group (Groups 1 and 2). * The vaccine seroresponse, seroprotection (hSBA titer \>=1:8), and antibody responses (GMTs) to serogroups A, C, Y, and W measured using hSBA on Day (D)0 (pre-vaccination) and D30 (+14 days) after vaccination with MenACYW Conjugate vaccine alone (Groups 1 and 2). * The antibody persistence (GMTs and vaccine seroprotection; hSBA titer \>=1:8) of meningococcal serogroups A, C, Y, and W before a booster dose in participants who received either MenACYW Conjugate vaccine or Menveo vaccine 3-6 years earlier. * The antibody persistence (GMTs and vaccine seroprotection; hSBA titer \>=1:8) of meningococcal serogroups A, C, Y, and W in participants who received either a single dose MenACYW Conjugate vaccine (participants randomized to MET59 Groups 1, 3, and 4) or Menveo vaccine (participants assigned to MET59 Group 2), as part of study MET50, or MET43 (participants randomized to MET59 Groups 1, 3 and 4). * To describe the vaccine seroresponse, seroprotection (hSBA titer \>=1:8), and antibody responses (GMTs) to the antigens present in MenACYW Conjugate vaccine, when MenACYW Conjugate vaccine was given concomitantly with meningococcal serogroup B (MenB) vaccine (Groups 3 and 4), compared to those when it was given alone (Group 1).

Study identification

NCT ID
NCT04084769
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
570 participants

Conditions and interventions

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 3, 2019 (Actual)
Primary completion
Sep 14, 2020 (Actual)
Completion
Sep 14, 2020 (Actual)
Last update posted
Sep 15, 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 15, 2025 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04084769 live on ClinicalTrials.gov.

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