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Novavax says its COVID-19 vaccine is 80% effective in children as young as 12

Novavax announced on Thursday that its Covid-19 vaccine has provedto be safe and effective in a study of 12- to 17-year-olds

Novavax says its COVID-19 vaccine is 80% effective in children as young as 12
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Novavax announced on Thursday that its Covid-19 vaccine has provedto be safe and effective in a study of 12- to 17-year-olds.

Novavax makes a protein-based vaccine, a different type than the most widely used shots, that's a late arrival to the Covid-19 arsenal. Its shots have been cleared for use in adults by regulators in Britain, Europe and elsewhere and by the World Health Organization, and are under review by the US Food and Drug Administration.

Armed with the new data, Novavax plans to soon seek expanded use of its shots down to age 12. Later this year, it plans to begin testing in younger children. The latest study enrolled 2,247 US children ages 12 to 17 last summer and found the two-dose vaccine was 80% effective at preventing symptomatic Covid-19 infection.

That was when the extra-contagious delta variant was circulating. The company said six vaccine recipients developed mild Covid-19 compared to 14 kids who received dummy shots. There were no serious infections.

In June, Maryland-based Novavax announced its vaccine was about 90% effective against symptomatic Covid-19 in a study of nearly 30,000 people in the US and Mexico. More recently, it has cited laboratory data suggesting the vaccine offers some protection against the more contagious omicron variant although a booster worked better.

The Novavax vaccine is made with lab-grown copies of the spike protein that coats the coronavirus, mixed with an immune-boosting chemical. That's similar to shots used for years against other diseases such as hepatitis B. It's a different technology than the Pfizer and Moderna options that deliver genetic instructions for the body to make its own spike protein.

Though the Pfizer-BioNTech shot is the only one authorized for U.S. children and teens, Moderna Inc. hopes to soon secure Food and Drug Administration clearance for its shot. Moderna has faced delays as regulators study the risk of myocarditis, a rare form of heart inflammation.

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