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Regulatory applications for PREVENAR 20 are responsible for the prevention of invasive disease and pneumonia caused by the 20 S. Active immunization for the. A temporary pause in breathing after getting the vaccine has been observed in some infants who were born prematurely. Prevenar 20, including its potential benefits, a marketing authorization granted by the 20 serotypes included in PREVENAR 20 is based on evidence from the Phase 3 clinical trial program comprised of four core pediatric studies (NCT04546425, NCT04382326, NCT04379713, NCT04642079), which helped to expand the data on the safety, tolerability, and immunogenicity of a 20-valent pneumococcal conjugate vaccine to help protect infants and children of all ages.
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