On a previous study conducted in Brazil. The MMR vaccine from 2 different producers had a mumps seroconversion much lower (71%) than the expected 95%, according to the package insert. This could indicate that a substantial proportion of children was not protected after MMR dose.
Given the above and considering: (1) future clinical study with the MMR vaccine produced entirely in Bio-Manguinhos/Fiocruz from technology transfer from GlaxoSmithKline (GSK), (2) the importance to the National Immunization Program (NIP) to provide the population a MMR vaccine to ensure high protection against mumps, similar to what occurs with measles and rubella components, it was considered essential to conduct a preliminary immunogenicity assessment of the MMR vaccine produced by BioManguinhos.
Study Type
OBSERVATIONAL
Enrollment
150
MMR (Mumps, Measles and Rubella)
Bio-Manguinhos/Fiocruz
Rio de Janeiro, Rio de Janeiro, Brazil
Immunoresponse after first dose
Assess the immunoresponse for measles, mumps and rubella after vaccination with MMR in children 12-23 months and 29 days old, in the routine of National Immunization Program (NIP) in health units in the city of Rio de Janeiro.
Time frame: 42 days
Immunoresponse after revaccination
To evaluate the immunoresponse after revaccination of children who did not seroconvert for any of the three components of the vaccine.
Time frame: 42 days
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