Moderna on Thursday asked U.S. regulators to authorize low doses of its COVID-19 vaccine for children younger than six, a long-awaited move toward potentially opening shots for millions of tots by summer.
Frustrated families are waiting impatiently for a chance to protect the littlest kids as all around them people shed masks and other public health precautions — even though highly contagious coronavirus mutants continue to spread.
Moderna submitted data to the Food and Drug Administration that it hopes will prove two low-dose shots can protect babies, toddlers and preschoolers — albeit not as effectively during the Omicron surge as earlier in the pandemic.
“There is an important unmet medical need here with these youngest kids,” Dr. Paul Burton, Moderna’s chief medical officer, told The Associated Press. Two kid-size shots “will safely protect them. I think it is likely that over time they will need additional doses. But we’re working on that.”
Now, only children ages five or older can be vaccinated in the U.S., using rival Pfizer’s vaccine, leaving 18 million younger tots unprotected.
Moderna’s vaccine isn’t the only one in the race. Pfizer is soon expected to announce if three of its even smaller-dose shots work for the littlest kids, months after the disappointing discovery that two doses weren’t quite strong enough.
Whether it’s one company’s shots or both, FDA vaccine chief Dr. Peter Marks said the agency will “move quickly without sacrificing our standards” in deciding if tot-sized doses are safe and effective.
While questions are swirling about what’s taking so long, Marks pointedly told lawmakers this week that the FDA can’t evaluate a product until a manufacturer completes its application. FDA will publicly debate the evidence with its scientific advisers before making a decision, and Marks said multiple meetings would be set to cover several expected applications.
“It’s critically important that we have the proper evaluation so that parents will have trust in any vaccines that we authorize,” Marks told a Senate committee.
If FDA clears vaccinations for the littlest, next the Centers for Disease Control and Prevention would have to recommend who needs them — all tots or just those at higher risk from COVID-19.
‘Kind of left behind’
Many parents are desperate for whichever vaccine gets to the scientific finish line first.
“We’ve been kind of left behind as everybody else moves on,” said Meagan Dunphy-Daly, a Duke University marine biologist whose six-year-old daughter is vaccinated — but whose three-year-old and 18-month-old sons are part of Pfizer’s trial.
The family continues to mask and take other precautions until it’s clear if the boys got real vaccine or dummy shots. If it turns out they weren’t protected in the Pfizer study and Moderna’s shots are cleared first, Dunphy-Daly said she’d seek them for her sons.
“I will feel such a sense of relief when I know my boys are vaccinated and that the risk of them getting a serious infection is so low,” she said.
The FDA will face some complex questions.
In a study of kids ages six months through five years, two Moderna shots — each a quarter of the regular dose — triggered high levels of virus-fighting antibodies, the same amount proven to protect young adults, Burton said. There were no serious side-effects, and the shots triggered fewer fevers than other routine vaccinations.
But the vaccine proved between about 40 per and 50 per cent effective at preventing symptomatic COVID-19 during the trial. Burton blamed the Omicron variant’s ability to partially evade vaccine immunity, noting that unboosted adults showed similarly less effectiveness against milder Omicron infections.
While no children became severely ill during the study, he said high antibody levels are a proxy for protection against more serious illness — and the company will test a child booster dose.
Another issue: So far in the U.S., Moderna’s vaccine is restricted to adults. Other countries have expanded the shot to kids as young as six. But months ago the FDA cited concern about a rare side-effect, heart inflammation, in teen boys, and it hasn’t ruled on Moderna’s earlier pediatric applications.
Burton said the FDA may consider its vaccine for children of all ages — but also might open it first to the youngest kids who have no other option. He said safety data from millions of older children given Moderna vaccinations abroad should help reassure parents.
A struggle to get kids vaccinated
Vaccinating eligible children against the coronavirus has been a struggle for many developed countries, with most North American and European countries starting their child inoculation drives between November and January.
Immunization rates are below 15 per cent among European children aged between five and nine, the youngest age group for which COVID-19 vaccines have been authorized there.
In the U.S., 28 per cent of children five to 11 as of April 20 were considered fully vaccinated, with 35 per cent having received at least one dose.
Canada has fared better than most Western countries in vaccinating the youngest eligible children, but federal and provincial health officials have said they would like to see the rate rise even more.
Nearly 41 per cent of Canadian kids aged five to 11 are fully vaccinated, according to Health Canada, and 56 per cent have received at least one dose.
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