NCT lookup
Pull any trial record directly from ClinicalTrials.gov.
Sponsor: Sanofi Pasteur, a Sanofi Company
Conditions: Meningitis, Meningococcal Infection
Interventions: Quadrivalent Meningococcal Polysaccharide (A, C, Y, and W-135) Tetanus Protein Conjugate, Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Inactivated Poliovirus and Haemophilus B Conjugate (Tetanus Toxoid Conjugate) Vaccine Combined (DTaP-IPV/Hib combined), M-M-RII-Measles, Mumps, and Rubella Virus Vaccine Live, Varicella Virus Vaccine Live, Pneumococcal 7-valent Conjugate Vaccine (Diphtheria CRM197 Protein)
Countries: United States
The purpose of this study was to evaluate the optimal vaccination schedule for a Quadrivalent Meningococcal Polysaccharide (A, C, Y and W-135) Tetanus Protein Conjugate Vaccine (MenACYW Conjugate vaccine) in order to provide an effective protein conjugate quadrivalent meningococcal vaccine in the population with the highest incidence of disease. Objectives: * To describe the safety profile of MenACYW Conjugate vaccine administered at 5 different schedules and concomitantly with routine pediatric vaccinations. * To describe the immunogenicity profile of MenACYW Conjugate vaccine administered at 5 different schedules and concomitantly with routine pediatric vaccinations. * To describe the immunogenicity profiles of selected licensed pediatric vaccines (Pentacel, Prevnar, M-M-RII, and Varivax) when administered either concomitantly with or without MenACYW Conjugate vaccine.
Sex: ALL
Age: 42 Days to 365 Days
Healthy volunteers: Yes
Study type: INTERVENTIONAL
Inclusion Criteria: * Groups 1, 2, 3, 6, and 7: Aged 42 to 89 days on the day of inclusion; Group 4: Aged 6 months (180 days ± 14 days) on the day of inclusion; Group 5: Aged 12 months (365 days + 14 days) on the day of inclusion. * Born at full term of pregnancy (greater than or equal to \[≥\] 37 weeks) and with a birth weight ≥2.5 kilogram (kg). * Informed consent form had been signed and dated by the parent or other legally acceptable representative. * Participant and parent/guardian were able to attend all scheduled visits and to be complied with all trial procedures. * Group 4 only: Prior receipt of Pentacel and Prevnar at 2 and 4 months; 1 or 2 doses of rotavirus vaccine; and 2 or 3 previous doses of hepatitis B vaccine. Group 5 only: Prior receipt of Pentacel and Prevnar at 2, 4, and 6 months; 2 or 3 doses of rotavirus vaccine; and 3 previous doses of hepatitis B vaccine. Exclusion Criteria: * Participation in another clinical trial investigating a vaccine, drug, medical device, or medical procedure in the 4 weeks preceding the first trial vaccination. * Planned participation in another clinical trial during the present trial period. * Receipt of any vaccine in the 4 weeks preceding the first trial vaccination. * Planned receipt of any vaccine in the 4 weeks following any trial vaccination, with the exception of influenza vaccine, which may be received 14 days before or after MenACYW Conjugate vaccine. * Previous vaccination against meningococcal disease with either the trial vaccine or another vaccine. * Receipt of blood or blood-derived products in the past 30 days, which might interfere with assessment of the immune response. * Known or suspected congenital or acquired immunodeficiency; or receipt of immunosuppressive therapy such as anti-cancer chemotherapy or radiation therapy; or long-term systemic corticosteroid therapy (prednisone or equivalent for more than 2 consecutive weeks). * Known personal or maternal seropositivity for human immunodeficiency virus (HIV), hepatitis B vaccine, or hepatitis C, as reported by the parent/guardian. * History of meningococcal infection, confirmed either clinically, serologically, or microbiologically. * At high risk for meningococcal infection during the trial. * Known systemic hypersensitivity to any of the vaccine components, or history of a life-threatening reaction to the vaccines used in the trial or to a vaccine containing any of the same substances. * Thrombocytopenia, as reported by the parent/guardian. * Bleeding disorder, or receipt of anticoagulants in the 3 weeks preceding inclusion, contraindicating intramuscular vaccination. * History of seizures. * Personal or family history of Guillain-Barré Syndrome (GBS). * Chronic illness that, in the opinion of the investigator, was at a stage where it might interfere with trial conduct or completion. Temporary contraindications were resolved before vaccination: * Febrile illness (temperature ≥38.0 degree Celsius \[≥100.4 degree Fahrenheit\]) or moderate or severe acute illness/infection (according to investigator judgment) on the day of vaccination. * Group 5 only: Receipt of oral or injected antibiotic therapy within the 72 hours prior to the study blood draw. Topical antibiotics or antibiotic drops were not included in this exclusion criterion. (Note: This did not applied to the other groups at this time, as they did not have a blood draw within 30 days of the initial visit.).
- Birmingham, Alabama, United States
- Tuscaloosa, Alabama, United States
- Jonesboro, Arkansas, United States
- Little Rock, Arkansas, United States
- Fountain Valley, California, United States
- Huntington Beach, California, United States
- Marietta, Georgia, United States
- Woodstock, Georgia, United States
- Bardstown, Kentucky, United States
- Crestview Hills, Kentucky, United States
- Louisville, Kentucky, United States
- Louisville, Kentucky, United States
- Bossier City, Louisiana, United States
- Clyde, North Carolina, United States
- Cleveland, Ohio, United States
- Pittsburgh, Pennsylvania, United States
- Barnwell, South Carolina, United States
- Clarksville, Tennessee, United States
- Fort Worth, Texas, United States
- Layton, Utah, United States
- Orem, Utah, United States
- Springville, Utah, United States
- Midlothian, Virginia, United States
- Spokane, Washington, United States
- Spokane, Washington, United States