Safety of a Quadrivalent Meningococcal Conjugate Vaccine Administered Concomitantly With Routine Pediatric Vaccines in Healthy Infants and Toddlers (MET41)

    Not Recruiting
  • End date
    Mar 24, 2023
  • participants needed
  • sponsor
    Sanofi Pasteur, a Sanofi Company
Updated on 10 October 2022
Accepts healthy volunteers


The primary objective of this study is to describe the safety profile of MenACYW conjugate vaccine and MENVEO® when administered concomitantly with routine pediatric vaccines in healthy infants and toddlers


Study duration per participant is approximately 16 months, which includes a safety follow-up contact at 6 months after the final vaccination

Condition Healthy Volunteers (Meningococcal Infection)
Treatment Hepatitis B vaccine, Pneumococcal 13-valent Conjugate Vaccine, Meningococcal polysaccharide (serogroups A,C,Y and W) tetanus toxoid conjugate vaccine (MenACYW conjugate vaccine), Meningococcal (Groups A, C, Y and W 135) Oligosaccharide Diphtheria CRM197 Conjugate Vaccine (MENVEO®), Diphtheria, Tetanus, Acellular Pertussis, Poliovirus and Haemophilus b Vaccine, Rotavirus Vaccine, Rotavirus Vaccine, Measles, Mumps, and Rubella Virus Vaccine, Varicella Virus Vaccine, Varicella Virus Vaccine
Clinical Study IdentifierNCT03673462
SponsorSanofi Pasteur, a Sanofi Company
Last Modified on10 October 2022

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