U.S. FDA advisers overwhelmingly back Moderna COVID vaccine for ages
6-17
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[June 15, 2022]
By Manas Mishra and Michael Erman
(Reuters) -Advisers to the U.S. Food and
Drug Administration on Tuesday unanimously recommended that the agency
authorize Moderna Inc's COVID-19 vaccine for children and teens aged 6
to 17 years of age.
Around 77 million people in the United States have received at least a
two-dose course of Moderna's vaccine, which has long been available for
people aged 18 and older.
The committee of outside experts is scheduled on Wednesday to consider
the Moderna shot for children under 6, and Pfizer and BioNTech's COVID
vaccine for children under 5 - and in both cases as young as 6 months.
There is unlikely to be significant immediate demand the Moderna shots
for 6- to 17-year olds. The Pfizer/BioNTech vaccine was authorized for
children aged 5 to 11 in October, and approval for teenagers preceded
that by months.
Yet only around 30% of those ages 5 to 11 and 60% of 12- to 17-year olds
are fully vaccinated in the United States, according to data from the
U.S. Centers for Disease Control and Prevention (CDC).
"I'd like to give parents as many choices as possible, and let them make
the decisions about this for their children," committee member and UC
Berkeley professor Dr. Arthur Reingold said at the meeting.
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A pharmacist holds a vial of the Moderna coronavirus disease
(COVID-19) vaccine in West Haven, Connecticut, U.S., February 17,
2021. REUTERS/Mike Segar
The FDA - which generally follows the recommendations
of its advisers but is not obligated to do so - is likely to
authorize the Moderna vaccine for ages 6-17 soon. The CDC also needs
to recommend the vaccine's use. A committee of its advisers is
scheduled to meet Friday and Saturday.
There have long been concerns that the Moderna vaccine, which is
given at a higher dose than the Pfizer/BioNTech shot, may cause
types of heart inflammation known as myocarditis and pericarditis at
higher rates, primarily in younger males.
Some countries in Europe have limited use of Moderna's vaccine for
younger age groups after surveillance suggested it was tied to a
higher risk of heart inflammation, and the FDA delayed its review of
the shot to assess the myocarditis risk.
U.S. regulators presented data at the meeting on Tuesday suggesting
that Moderna's vaccine may have a higher risk of heart inflammation
in young men, but said the findings were not consistent across
various safety databases and were not statistically significant,
meaning they might be due to chance.
(Reporting by Manas Mishra in Bengaluru; Additional reporting by
Michael Erman in New Jersey; Editing by Jason Neely and Bill Berkrot)
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