U.S.
FDA set to authorize Pfizer COVID-19 shot for ages 12-15 early next week
- NYT
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[May 04, 2021]
(Reuters) - The U.S. Food and Drug
Administration is preparing to authorize Pfizer Inc and German partner
BioNTech SE's COVID-19 vaccine for adolescents aged between 12 and 15
years by early next week, the New York Times reported on Monday, citing
federal officials familiar with the agency's plans.
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An
approval is highly anticipated after the drugmakers said in March
that the vaccine was found to be safe, effective and produced robust
antibody responses in 12- to 15-year-olds in a clinical trial.
Responding to a Reuters request for comment, the FDA said its review
of expanding the vaccine's emergency use authorization is ongoing,
but did not provide further details.
The vaccine has already been cleared in the United States for people
aged 16 and above. (https://reut.rs/3nLH8Fj)
Pfizer declined to comment on the NYT report.
The U.S. Centers for Disease Control (CDC) Director Rochelle
Walensky said earlier in April that the vaccine could be approved by
mid-May.
If an approval for the 12-15 year olds is granted, the CDC's vaccine
advisory panel will likely meet the following day to review the
clinical trial data and make recommendations for the vaccine's use
in adolescents, the report added. (https://nyti.ms/3eclRld)
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A potential approval of the vaccine would boost the country's
immunization drive and help allay fears of parents anxious to
protect their children from COVID-19.
Moderna Inc and Johnson & Johnson are also testing their vaccines in
12- to 18-year olds, with data from Moderna's trial expected to come
soon.
Pfizer and Moderna have also launched trials in even younger
children, aged six months to 11 years old. Both companies have said
they hope to be able to vaccinate children under 11 as soon as early
2022.
(Reporting by Trisha Roy in Bengaluru; Editing by Devika Syamnath)
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