The Food and Drug Administration has greenlit updated COVID-19 vaccine doses for children under the age of 5, but the change to the authorized vaccination regimens is far from straightforward. This may further hamstring efforts to vaccinate the youngest Americans, which are already off to an abysmal start.
After months of availability, only about 3 percent of infants and toddlers 6 months to 2 years old have completed a primary series. Just 6.5 percent have gotten at least one shot, according to data from the Centers for Disease Control and Prevention. For those aged 2 to 4 years, just under 5 percent have completed a primary series, with 9 percent having gotten at least one dose.
It was back in June when the FDA authorized—and the CDC endorsed—small doses of both Moderna’s and Pfizer’s COVID-19 vaccines for children as young as 6 months old.
- For Moderna’s vaccine, infants 6 months to adolescents 17 years could get a primary series of two doses, one month apart.
- For Pfizer’s vaccine, infants from 6 months to children through age 4 years could get a primary series of three doses, the second being given three weeks after the first and the third being given at least eight weeks after the second. (Pfizer’s vaccine was previously available to children 5 years old and older.)
This fall, the FDA authorized an “updated” bivalent vaccine for use as a booster dose in people aged 5 years and above. The bivalent shot targets both the original version of SARS-CoV-2 and the coronavirus omicron subvariants BA.4/5, which were dominant during the summer months. Now, genetic offshoots of BA.5 are dominating circulation. Recent real-world effectiveness data suggests that the bivalent booster offers up to 56 percent more protection against symptomatic COVID-19 infection than protection from the original boosters.

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