FDA advisory group recommends Moderna booster for emergency use

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FDA advisory group recommends Moderna booster for emergency use
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JUST IN: FDA advisory panel votes to recommend Moderna booster shots for emergency use authorization for certain at-risk groups.

Jacqueline Miller, therapeutic area head for infectious diseases at Moderna, said in her presentation to the committee that the company chose the half dose because it wanted to use the lowest dose possible needed to induce an immune response.

compared to people who received their vaccinations several months later, Miller said. Nearly all of these breakthrough infections were caused by the delta variant."We are concerned about the breakthrough disease that we’ve been observing in the participants in the [original clinical trial], and particularly the breakthrough cases that we’re starting to see in severe disease in the older adults," Miller said.

However, the booster trial didn’t include enough participants to evaluate whether the extra dose raised the risk forMyocarditis, or inflammation of the heart muscle, has been linked to both Moderna and Pfizer’s Covid-19 vaccines. The condition is rare and mostly commonly seen in men under 30. In data from Israel, where 3.7 million people have received a Pfizer booster shot, 17 cases of myocarditis were reported, said Dr. Sharon Alroy-Preis, director of public health services for Israel’s Ministry of Health, who presented Thursday.

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