Pfizer’s vaccine that protects infants from respiratory syncytial virus could receive Food and Drug Administration approval by the end of this summer.
Pfizer on Tuesday said the FDA is reviewing the vaccine on an expedited basis. The agency is expected to make a decision on whether to clear the shot in August, just before respiratory virus season.
The single-dose vaccine is administered to expectant mothers in the late second to third trimester of their pregnancy. The antibodies triggered by the shot are passed to the fetus, and protect infants against RSV from birth through the first six months of life, when they are most vulnerable.
The vaccine was 82% effective at preventing severe disease from RSV in newborns during the first 90 days of life, according to data from Pfizer’s clinical trial. The shot was about 70% effective during the first six months of the baby’s life.