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Completed Phase 4 Interventional Accepts healthy volunteers Results available

Study of Menactra® in US Adolescents When Administered Concomitantly With Tdap Vaccine

ClinicalTrials.gov ID: NCT00777257

Public ClinicalTrials.gov record NCT00777257. 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 Sep 3, 2026, 3:48 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 Meningococcal (Groups A, C, Y, and W-135) Diphtheria Toxoid Conjugate Vaccine (Menactra®) in Adolescents in the US When Administered Concomitantly With Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (Tdap Vaccine)

Brief summary

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

The purpose of this study was to evaluate the immunogenicity and safety of the concomitant administration of Menactra® vaccine and Tdap vaccine in adolescents aged 11 to 17 years. Primary Objective: To determine whether concomitant administration of two vaccines, Tdap and Menactra®, induces antibody responses that are similar to those observed when each vaccine is given separately. Secondary Objective: To compare the rates of injection site reactions at the Tdap injection site after Tdap and Menactra® vaccines are administered concomitantly to the corresponding rates of reactions when Tdap vaccine is administered alone.

Study identification

NCT ID
NCT00777257
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
1,345 participants

Conditions and interventions

Eligibility (public fields only)

Age range
11 Years to 17 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
Mar 31, 2005
Primary completion
Feb 28, 2007
Completion
Aug 31, 2007
Last update posted
Feb 13, 2014

2005 – 2007

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Not listed Jonesboro Arkansas 72401
Not listed Little Rock Arkansas 72205
Not listed Boulder Colorado 80303
Not listed Marietta Georgia 30062
Not listed Woodstock Georgia 30189
Not listed Bardstown Kentucky 40004
Not listed Baltimore Maryland 21201
Not listed Woburn Massachusetts 01801
Not listed Albuquerque New Mexico 87108
Not listed Syracuse New York 13210
Not listed Raleigh North Carolina 27609
Not listed Sylva North Carolina 28779
Not listed Akron Ohio 44308
Not listed Cleveland Ohio 44118
Not listed Columbus Ohio 43205
Not listed Dayton Ohio 45404
Not listed Pittsburgh Pennsylvania 15241
Not listed Sellersville Pennsylvania 18960
Not listed Kingsport Tennessee 37660
Not listed Spokane Washington 99202

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00777257, 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 Feb 13, 2014 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00777257 live on ClinicalTrials.gov.

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