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Completed Phase 2 Interventional Accepts healthy volunteers Results available

Study of Menactra® in Children Aged 4 to 6 Years When Administered Concomitantly With a Fifth Dose of DAPTACEL®

ClinicalTrials.gov ID: NCT00355121

Public ClinicalTrials.gov record NCT00355121. 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 2, 2026, 6:36 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 Meningococcal (Serogroups A, C, Y and W-135) Polysaccharide Diphtheria Toxoid Conjugate Vaccine (Menactra®) in Children Aged 4 to 6 Years in the US When Administered Concomitantly With a Fifth Dose Diphtheria and Tetanus Toxoids and Acellular Pertussis Vaccine Adsorbed.

Brief summary

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

The purpose of this study is to evaluate the immunogenicity and safety of the concomitant administration of Menactra® vaccine and DAPTACEL® vaccine. The main objectives are: Immunogenicity: To evaluate the antibody responses to both vaccines when Menactra vaccine is given concomitantly with DAPTACEL® compared to when either vaccine is given alone. Safety: To evaluate the rate of local and systemic reactions when DAPTACEL® and Menactra vaccines are administered concomitantly compared to when each vaccine is given alone.

Study identification

NCT ID
NCT00355121
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sanofi
Industry
Enrollment
882 participants

Conditions and interventions

Eligibility (public fields only)

Age range
4 Years to 7 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 30, 2006
Primary completion
May 31, 2009
Completion
Jun 30, 2009
Last update posted
Aug 23, 2011

2006 – 2009

United States locations

U.S. sites
26
U.S. states
14
U.S. cities
26
Facility City State ZIP Site status
Not listed Little Rock Arkansas 72205
Not listed Boulder Colorado 80304
Not listed Atlanta Georgia 30322
Not listed Layton, UT 84041 Georgia 30062
Not listed Bardstown Kentucky 40004
Not listed Woburn Massachusetts 01801
Not listed Bridgeton Missouri 63044
Not listed St Louis Missouri 63141
Not listed Albuquerque New Mexico 87108
Not listed Rochester New York 14620
Not listed Syracuse New York 13210
Not listed Akron Ohio 44308
Not listed Cincinnati Ohio 45229
Not listed Columbus Ohio 43205
Not listed University Heights Ohio 44118
Not listed Pittsburgh Pennsylvania 15241
Not listed Sellersville Pennsylvania 18960
Not listed Kingsport Tennessee 37660
Not listed Layton Utah 84041
Not listed Ogden Utah 84405
Not listed Pleasant Grove Utah 84062
Not listed Provo Utah 84604
Not listed Salt Lake City Utah 84123
Not listed South Jordan Utah 84095
Not listed Norfolk Virginia 23510
Not listed Spokane Washington 99220

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 NCT00355121, 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 Aug 23, 2011 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00355121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →