But the timeline for FDA approval is still up in air.
A Moderna official said that it will take until about May 9 to get all of the paperwork to the government agency, and then it’s on the FDA to make a decision.: "We believe mRNA-1273 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 said that the lower effectiveness levels were related to the fact that 80 percent of the infections they saw were the Omicron variant, which causes more breakthrough cases.that has been a concern and no sign that the vaccine causes more high fevers than other routine vaccines.It depends on a few factors.
so that they can compare the two and possibly release them at the same time, like they did with the adult vaccine. That would obviously also take longer.
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