Meningococcal polysaccharide diphtheria toxoid conjugate
Biological0.5 mL, Intramuscular
Other names: Menactra®
NCT Number: NCT00771849
The study investigated safety profile and the antibody responses to an experimental tetravalent meningococcal diphtheria conjugate vaccine (Menactra®) in children who have received a monovalent meningococcal C conjugate vaccine at least one year previously.
Primary objective:
To describe and compare the Serum Bactericidal Assay (SBA) antibody response for serogroup C in participants receiving Menactra® to the serogroup C antibody response in a control group of participants receiving a licensed Haemophilus Influenzae Type b (Hib) conjugate vaccine 28 days following vaccination.
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Notify Me2 year–4 year
All sexes
Interventional
Phase 2
London, United Kingdom
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
0.5 mL, Intramuscular
Other names: Menactra®
0.5 mL, Intramuscular
Other names: Hiberix®
Time frame: Day 0 (before) and 28 days post-vaccination
Time frame: 28 days post-vaccination
Sanofi Pasteur, a Sanofi Company
Industry
Antibody Responses for Serogroup C After One Dose of an Experimental Tetravalent (A, C, Y, and W-135) Meningococcal Diphtheria Toxoid Conjugate Vaccine Versus a Non-meningococcal Control Vaccine in Children Who Have Previously Received a Monovalent Meningococcal C Conjugate Vaccine
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