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Pfizer Resubmits Application for COVID-19 Vaccine for Children Under 5

The FDA is meeting on June 15 to discuss emergency use authorization.

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Corinne Reichert Senior Editor
Corinne Reichert (she/her) grew up in Sydney, Australia and moved to California in 2019. She holds degrees in law and communications, and currently writes news, analysis and features for CNET across the topics of electric vehicles, broadband networks, mobile devices, big tech, artificial intelligence, home technology and entertainment. In her spare time, she watches soccer games and F1 races, and goes to Disneyland as often as possible.
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Corinne Reichert
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Children under 5 may be able to get vaccinated soon.

Sarah Tew/CNET

Pfizer and its partner BioNTech have resubmitted their application to have a three-dose COVID-19 vaccine for children aged 6 months to 4 years old gain emergency use authorization from the FDA. The FDA reportedly accepted Pfizer's application to look at the data Wednesday.

"Pfizer and BioNTech completed a rolling application to the US Food and Drug Administration for emergency use authorization," Pfizer said in an emailed statement.

Pfizer had previously asked the FDA to authorize its vaccine for kids 6 months to 4 years in February but postponed its request pending more data. Pfizer said last week that trials showed its three-dose vaccine produced a strong immune response in children under 5.

Ahead of the expected submission, the FDA last week said its Vaccines and Related Biological Products Advisory Committee would meet on June 15 to discuss emergency use authorization requests for Pfizer and Moderna vaccines for children aged 6 months and over.

Moderna asked for approval at the end of April. Moderna's vaccine for children under 5 involves two doses of its 25 microgram vaccine (one-fourth of the volume of the adult Moderna dose). Pfizer's is three 3-microgram doses -- one-tenth of the dose for adults.

"We recognize parents are anxious to have their young children vaccinated against COVID-19, and while the FDA cannot predict how long its evaluation of the data and information will take, we will review any EUA request we receive as quickly as possible using a science-based approach," the FDA told ABC News in a statement.

The FDA didn't immediately respond to a request for comment. The vaccine would have to be approved by the committee before the full FDA, followed by CDC approval.

The information contained in this article is for educational and informational purposes only and is not intended as health or medical advice. Always consult a physician or other qualified health provider regarding any questions you may have about a medical condition or health objectives.