The primary objectives of this study are: * To describe the antibody response to meningococcal serogroups A, C, W, and Y measured by serum bactericidal assay using baby rabbit complement (rSBA) before and after a single dose of MenACYW conjugate vaccine * To describe the antibody response to meningococcal serogroups A, C, W, and Y measured by serum bactericidal assay using human complement (hSBA) before and after a single dose of MenACYW conjugate vaccine * To describe the antibody responses against tetanus toxoid at baseline and after a single dose of MenACYW conjugate vaccine * To describe the safety profile of a single dose of MenACYW conjugate vaccine
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Percentage of Participants With Serum Bactericidal Assay Using Baby Rabbit Complement (rSBA) Antibody Titers Greater Than or Equal to (>=) 1:8 Against Meningococcal Serogroups A, C, W, and Y
Timeframe: Day 30 post-dose
Geometric Mean Titers Against Meningococcal Serogroups A, C, W, and Y Measured by rSBA
Timeframe: Day 30 post-dose
Geometric Mean Titers Against Meningococcal Serogroups A, C, W, and Y Measured by Serum Bactericidal Assay Using Human Complement (hSBA)
Timeframe: Day 30 post-dose
Geometric Mean Concentrations (GMCs) of Antibodies Against Tetanus Toxoid
Timeframe: Pre-dose Day 0 and Day 30 post-dose
Percentage of Participants Who Achieved Seroprotective Levels
Timeframe: Pre-dose Day 0 and Day 30 post-dose
Number of Participants With Unsolicited Systemic Adverse Events (AEs)
Timeframe: Within 30 minutes post-dose
Number of Participants With Solicited Injection Site Reactions and Systemic Reactions
Timeframe: Up to 7 days post-dose
Number of Participants With Unsolicited Non-Serious Adverse Events
Timeframe: Up to Day 30 post-dose
Number of Participants With Serious Adverse Events (SAEs)
Timeframe: From Day 0 up to end of study, approximately 44 days