Pfizer submits COVID-19 shot for children under 5 for FDA authorization
Pfizer has asked U.S. regulators to clear its COVID-19 vaccine for emergency use in children under the age of 5, an effort to extend protection against the virus to the country’s youngest.
The drugmaker and BioNTech SE finalized their rolling application to the Food and Drug Administration for emergency-use authorization of their vaccine in kids ages 6 months through 4 years, the companies said in a statement on Wednesday. The vaccine partners began the submission process in February.
Pfizer and BioNTech announced in late May that a three-shot regimen was highly effective and prompted a strong immune response in children under age 5, based on early results from a highly anticipated trial that is likely to pave the way for infants and toddlers to be immunized.
The preliminary analysis found that the vaccine was 80.3% effective in preventing COVID infections among young children, with 10 infections occurring among all participants. Final results will be determined once 21 children enrolled in the study have been infected, according to the companies.
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In February, Pfizer and BioNTech launched a rolling review of data from the trial of 1,678 children under the age of 5. The three-dose vaccine regimen was well-tolerated, with a safety profile similar to that of the placebo, and most side effects were mild or moderate.
The full submission includes data on the product’s safety, efficacy and ability to prompt an immune response. Children under the age of 5 were given a series of three doses, each 3 micrograms, or one-tenth the amount given to adults.
With the submission now complete, attention will turn to a forthcoming FDA advisory committee meeting on June 15. The panel of experts will convene to discuss the risks and benefits of the Pfizer-BioNTech and Moderna vaccines in the youngest children, and provide a recommendation to U.S. regulators as to whether they should be cleared for emergency use.
Pfizer said the companies also plan to submit the data to the European Medicines Agency and other regulators around the world.
