It has been nine months since the Pfizer-BioNTech vaccine became available to individuals ages 16 and older under an emergency use authorization from the U.S. Food and Drug Administration. It has been four months since the FDA granted similar authorization for those 12 to 15 years of age.
At a time when COVID-19 cases in children are on the rise, according to the Centers for Disease Control, Pfizer-BioNTech released results Sept. 20 of a pivotal study on the vaccine’s effectiveness and safety in children ages 5 to 11.
The trial gathered data from 2,298 participants and found that a 10 µg dose – about a third of the adult dose – built robust neutralizing antibody responses in children, similar to those seen in adults. As of Tuesday, the trial data was shared with the FDA for initial review, with a formal emergency use authorization request to be submitted in the coming weeks.
Under the anticipated timeline, an announcement from the FDA is expected to come between Halloween and Thanksgiving.
With a children’s vaccine likely around the corner, UVA Today gained insight on the Pfizer study and vaccine rollout from Dr. William Petri, vice chair for research in the UVA Department of Medicine, a chaired professor of infectious disease and international health and the head of a lab studying COVID-19 vaccines and treatments.
Q. How did Pfizer conduct its study on children under 12?
A. The approach to all COVID-19 vaccine tests has been one of age de-escalation, starting with adults, and only when proven safe and effective are the vaccines tested on children.

