Immunogenicity and Safety Study of an Investigational Quadrivalent Meningococcal Conjugate Vaccine Administered Concomitantly With Routine Pediatric Vaccines in Healthy Infants and Toddlers

Who is this study for? Patients with Meningococcal Infection
Status: Completed
Location: See all (47) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The primary objective of this study is to demonstrate the non-inferiority of the vaccine seroresponse to meningococcal serogroups A, C, Y, and W following administration of 2 doses of MenACYW conjugate vaccine compared to 2 doses of MENVEO® when given concomitantly with routine pediatric vaccines to infants and toddlers 6 to 7 months of age and 12 to 13 months of age. The secondary objectives of the study are: * To demonstrate the non-inferiority of the percentage of participants with antibody titers to meningococcal serogroups A, C, Y, and W ≥ 1:8 following administration of 2 doses of MenACYW conjugate vaccine compared to 2 doses of MENVEO® when given concomitantly with pediatric routine vaccines to infants and toddlers at 6 to 7 months of age and 12 to 13 months of age. * To describe the antibody response against meningococcal serogroups A, C, Y, and W 30 days after the second vaccination at 12 to 13 months of age with MenACYW conjugate vaccine or MENVEO®. * To describe the antibody response against meningococcal serogroups A, C, Y, and W 30 days and 6 months after the first vaccination at 6 to 7 months of age with MenACYW conjugate vaccine or MENVEO®. * To describe the antibody response against meningococcal serogroups A, C, Y, and W 30 days after the second vaccination at 20 to 23 months of age with MenACYW conjugate vaccine or Menactra®.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6 months
Maximum Age: 1
Healthy Volunteers: t
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• Aged 6 to 7 months (168 to 224 days) or 17 to 19 months on the day of the first visit

• Informed consent form has been signed and dated by the parent(s) or other guardian and by an independent witness if required by local regulations

• Subject and parent/guardian are able to attend all scheduled visits and to comply with all trial procedures

• For subjects 6 to 7 months of age at enrollment (Group 1 and Group 2), documented history of having received 2 doses of diphtheria, tetanus and acellular pertussis (DTaP), Haemophilus influenza type B (Hib), inactivated poliovirus (IPV), pneumococcal, hepatitis B (for children who received hepatitis B at 2 and 4 months of age, prior receipt of 3 doses of hepatitis B), and rotavirus vaccines

• For subjects to be enrolled at 17 to 19 months of age (Group 3 and Group 4), documented history of having received all routine pediatric vaccines recommended by the Advisory Committee on Immunization Practices (ACIP) up to the age of enrollment

Locations
United States
Alabama
Alabama Clinical Therapeutics Site Number : 8400036
Birmingham
Southeastern Pediatric Associates Site Number : 8400009
Dothan
Arizona
MedPharmics, LLC - Phoenix Site Number : 8400013
Phoenix
California
Emmaus Research Center, Inc Site Number : 8400019
Anaheim
Coast Clinical Trials, LLC Site Number : 8400073
Bellflower
Matrix Clinical Research Site Number : 8400082
Gardena
Madera Family Med Group Site Number : 8400065
Madera
Florida
Next Phase Research Alliance Site Number : 8400044
Homestead
PAS Research Site Number : 8400101
Land O' Lakes
Axcess Medical Research Site Number : 8400021
Loxahatchee Groves
Biomedical Research LLC Site Number : 8400041
Miami
Y and L Advance Health Care, Inc D/B/A Elite Clinical Res Site Number : 8400046
Miami
Crystal Biomedical Research Site Number : 8400034
Miami Lakes
PAS Research Site Number : 8400059
Tampa
Georgia
Omega Pediatrics Site Number : 8400093
Roswell
Idaho
Snake River Research, PLLC Site Number : 8400058
Idaho Falls
Illinois
Eagle Clinical Research Site Number : 8400094
Chicago
Kentucky
All Children Pediatrics Site Number : 8400024
Louisville
Brownsboro Park Pediatrics Site Number : 8400039
Louisville
Louisiana
Meridian Clinical Research, LLC Site Number : 8400035
Baton Rouge
Velocity Clinical Research Site Number : 8400016
Metairie
Willis-Knighton Physician Network Site Number : 8400075
Shreveport
Massachusetts
Pediatric Associates of Fall River Site Number : 8400112
Fall River
Maryland
Victory Clinical Research Site Number : 8400026
Baltimore
Missouri
Craig Spiegel, MD Site Number : 8400023
Bridgeton
North Carolina
Wilmington Health Site Number : 8400054
Wilmington
Nebraska
Meridian Clinical Research Site Number : 8400097
Hastings
Midwest Childrens Health Research Institute Site Number : 8400111
Lincoln
Midwest Childrens Health Research Institute Site Number : 8400117
Lincoln
New Mexico
MedPharmics Inc Site Number : 8400006
Albuquerque
New York
Advantage Clinical Trials Site Number : 8400069
New York
Ohio
Ohio Pediatric Research Site Number : 8400022
Dayton
PriMed Clinical Research Site Number : 8400008
Dayton
Oklahoma
Oklahoma State University - Center for Health Sciences Site Number : 8400110
Tulsa
Oregon
Cyn3rgy Research Site Number : 8400010
Gresham
Pennsylvania
Allegheny Health and Wellness Pavilion Site Number : 8400025
Erie
Kid's Way Pediatrics Site Number : 8400015
Hermitage
South Carolina
Coastal Pediatric Research Charleston Site Number : 8400002
Charleston
Coastal Pediatric Research Charleston Site Number : 8400011
Charleston
Tribe Clinical Research Site Number : 8400118
Greenville
Tennessee
Pediatric Clinical Trials Tullahoma Site Number : 8400106
Tullahoma
Texas
Tekton Research Site Number : 8400047
Beaumont
Mercury Clinical Research, Inc. Site Number : 8400088
Dickinson
Clinical Trial Network - 7080 Southwest Fwy Site Number : 8400037
Houston
Tekton Research, Inc. Site Number : 8400040
San Antonio
Other Locations
Puerto Rico
Investigational Site Number : 6300102
Guayama
Investigational Site Number : 6300014
San Juan
Time Frame
Start Date: 2018-10-04
Completion Date: 2023-10-20
Participants
Target number of participants: 950
Treatments
Experimental: Group 1
MenACYW conjugate vaccine + routine pediatric vaccines at 6 to 7 months of age and 12 to 13 months of age
Active_comparator: Group 2
MENVEO® + routine pediatric vaccines at 6 to 7 months of age and 12 to 13 months of age
Experimental: Group 3
MenACYW conjugate vaccine at 17 to 19 months of age and 20 to 23 months of age
Active_comparator: Group 4
Menactra® at 17 to 19 months of age and 20 to 23 months of age
Sponsors
Leads: Sanofi Pasteur, a Sanofi Company

This content was sourced from clinicaltrials.gov