Advisers to the U.S Food and Drug Administration on Wednesday unanimously recommended the agency authorize COVID-19 vaccines from Moderna Inc (MRNA.O) and Pfizer Inc (PFE.N)/BioNTech SE (22UAy.DE) for millions of the youngest American children.
The committee’s recommendation is an important step toward immunizing children under the age of 5 and as young as 6 months old who have not yet been eligible for the shots.
The FDA is likely to authorize the shots soon. The U.S. government is planning for a June 21 start to its under-5 vaccination campaign should the vaccines receive FDA authorization, White House COVID-19 response coordinator Ashish Jha said last week.
COVID-19 is generally more mild in children than adults, but FDA officials told the panel that the number of U.S. COVID deaths so far in small children - roughly 442 under age 5 - “compared terribly” to the 78 deaths reported during the swine flu pandemic of 2019-2010.
“I think we have to be careful that we don’t become numb to the number of pediatric deaths because of the overwhelming number of older deaths,” FDA official Peter Marks told the panel.
Public health officials and experts say that even though a large portion of small children were infected during the winter surge in cases driven by the Omicron variant of the coronavirus, natural immunity wanes over time and vaccinations should help prevent hospitalizations and deaths when cases rise again.
The two vaccines are not interchangeable. Moderna’s vaccine for children under 6 is a two-dose, 25 microgram vaccine, with the shots given about four weeks apart. The Pfizer/BioNTech vaccine for the youngest children is a lower dose, 3-shot regimen given over at least 11 weeks.
Several panelists at the meeting voiced concerns that the Pfizer/BioNTech vaccine was not substantially protective until children received the third shot, noting that parents might believe their children were protected while awaiting that last dose.