Table 5.
Vaccine | Bexsero® | Trumenba® |
---|---|---|
Composition | fHbp variant1 (subfamily B): 50 µg NHBA 50 µg NadA 50 µg PorA P1.4 25 µg |
Lipidated proteines of:fHbp variant1 (subfamily B): 60 µg fHbp variant3 (subfamily AB): 60 µg |
Licensure | Europe (EMA) (2013): ≥2 mo USA FDA (2015): ≥10 y | Europe (EMA) (20173): ≥10 y mo USA FDA (2015) ≥ 10 y |
Schedule <10 y) | 2 Mo-2y: 2 + 1 > 2 y-10y: 2 doses (0–2mo) |
- |
Schedule ≥ 10 y | > 10 y: 2 doses (0–1mo); booster unknown | 2 doses (0–6mo) or 3 doses (0–1/2-6mo); booster unknown |
Persistence of the immune response | Infants and toddlers 24–36 mo after booster Adolescents 4–7.5 years |
4–5 y |
Estimation of strain converge | 78% (CI 63–90) | 91% (71.5–99.3)* |
Impact on acquisition of carriage | No | No |
Protection against non-B isolates | Yes | Yes |
*Range of coverage against reference strains.