The
FDA's reviewers said in briefing documents published on Friday
evening that the vaccine had generated a similar immune response
in the children than that observed in adults in previous trials.
"Available data support the effectiveness of the Moderna
COVID-19 Vaccine in preventing symptomatic COVID-19 in pediatric
age groups from 6 months through 17 years of age," the FDA staff
said.
The FDA staff also said the vaccine generally had a similar side
effect profile in children as seen in adults, although younger
children had fevers more frequently.
Both of the messenger RNA-based COVID-19 vaccines made by
Moderna and Pfizer/BioNTech have been linked to rare instances
of a type of heart inflammation called myocarditis, particularly
in young men.
Some countries in Europe have limited the use of Moderna's shots
for younger age groups after some studies showed that it was
tied to a higher risk of the heart inflammation.
The FDA said myocarditis is a known risk associated with the
vaccine, but that the drugmaker's pediatric trials were not
large enough to quantify the frequency of the rare heart
inflammation in pediatric age groups.
The Pfizer/BioNTech vaccine is already authorized in the U.S.
for people aged 5 and older. The U.S. Centers for Diseases
Control and Prevention (CDC) said in May that reports of
myocarditis after that vaccine have been much lower in 5- to
11-year-old boys than in adolescents and young men, representing
only a slightly elevated rate than normal.
(Reporting by Michael Erman in New Jersey; editing by Grant
McCool)
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