Pfizer said the request 'is an important step in our ongoing effort against #COVID19.'
Pfizer and BioNTech announced Thursday that they had submitted an emergency request to the U.S. Food and Drug Administration for authorization of the companies' two-dose"With new cases in children in the U.S. continuing to be at a high level, this submission is an important step in our ongoing effort against #COVID19," Pfizer tweeted."We’re committed to working with the FDA with the ultimate goal of helping protect children against this serious public health threat.
During the trial, children were given two smaller doses than those given to people who are 12 and older. Pfizer and BioNTech said the shots produced antibody responses and side effects that were comparable to those seen in a similar study of people 16 to 25 who received the full dose of the vaccine.for its vaccine for adults last November.
While kids generally get significantly less ill from the coronavirus than adults do, in very rare instances, there can be severe orPfizer's shots are one of three that are being used in the U.S., along with Moderna's two-dose vaccine and Johnson & Johnson's single-shot vaccine. Moderna and Johnson & Johnson are still in the research phase of the shots being used for children 5 to 11.
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