Efficacy and Safety of a Bivalent RSV Prefusion F Vaccine in Older Adults

In a phase 3 trial, adults (≥60 years of age) received one 120-μg dose of RSVpreF vaccine (17,215) or placebo (17,069). Vaccine efficacy against RSV-associated lower respiratory tract illness was 67 to 86%.

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Veröffentlicht in:The New England journal of medicine 2023-04, Vol.388 (16), p.1465-1477
Hauptverfasser: Walsh, Edward E., Pérez Marc, Gonzalo, Zareba, Agnieszka M., Falsey, Ann R., Jiang, Qin, Patton, Michael, Polack, Fernando P., Llapur, Conrado, Doreski, Pablo A., Ilangovan, Kumar, Rämet, Mika, Fukushima, Yasushi, Hussen, Nazreen, Bont, Louis J., Cardona, Jose, DeHaan, Elliot, Castillo Villa, Giselle, Ingilizova, Marinela, Eiras, Daniel, Mikati, Tarek, Shah, Rupal N., Schneider, Katherine, Cooper, David, Koury, Kenneth, Lino, Maria-Maddalena, Anderson, Annaliesa S., Jansen, Kathrin U., Swanson, Kena A., Gurtman, Alejandra, Gruber, William C., Schmoele-Thoma, Beate
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Sprache:eng
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Zusammenfassung:In a phase 3 trial, adults (≥60 years of age) received one 120-μg dose of RSVpreF vaccine (17,215) or placebo (17,069). Vaccine efficacy against RSV-associated lower respiratory tract illness was 67 to 86%.
ISSN:0028-4793
1533-4406
DOI:10.1056/NEJMoa2213836