Moderna announced Thursday that it has asked the U.S. Food and Drug Administration to authorize the emergency use of its COVID-19 vaccine for children under the age of 6.
It’s the first vaccine maker to seek U.S. authorization of a COVID-19 shot for that age group.
“We believe mRNA-1273 [the Moderna vaccine] will be able to safely protect these children against SARS-CoV-2, which is so important in our continued fight against COVID-19, and will be especially welcomed by parents and caregivers,” Moderna CEO Stéphane Bancel said in a statement.
A company official said Moderna would have all relevant data to the FDA by May 9, The New York Times reported.
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How well does the vaccine work?
The two 25-microgram doses of the vaccine for children younger than 6 are smaller than the two 100-microgram doses for adults, but tests among children ages 6 months to under 6 showed a “robust neutralizing antibody response” and a “favorable safety profile,” according to Moderna.
The company also said that preliminary analysis of lab tests during the Omicron wave showed the vaccine’s efficacy against infection was 51% among children younger than 2 and 37% among children from 2 to 5 years old, CBS News reported.
“These efficacy estimates are similar to vaccine efficacy estimates in adults against Omicron after two doses,” the company said in its statement.
What’s next?
For now, FDA authorization of the Moderna vaccine is limited to adults. Along with the new request, the company has also asked for
