Albuquerque Journal

FDA advisers back Moderna’s COVID-19 vaccine for kids age 6-17

Jury is still out on shots for children under 5

- BY MIKE STOBBE

NEW YORK — A government advisory panel Tuesday endorsed a second brand of COVID-19 vaccine for schoolage children and teens.

The Food and Drug Administra­tion’s outside experts voted unanimousl­y that Moderna’s vaccine is safe and effective enough to give kids ages 6 to 17. If the FDA agrees, it would become the second option for those children, joining Pfizer’s vaccine.

The same FDA expert panel will meet Wednesday to consider tot-sized shots from Moderna and Pfizer for the littlest kids, those under 5.

Moderna’s COVID-19 vaccine has long been available for adults in the U.S. and elsewhere, and more than three dozen countries offer it to older children, too. If the FDA authorizes Moderna’s vaccine for teens and younger children, the Centers for Disease Control and Prevention will next decide whether to formally recommend the shots.

The Massachuse­tts company is seeking clearance for two doses, and plans to later offer a booster. Tuesday’s vote was only for two doses — full-strength for 12-17 and half-sized doses for those 6-11.

“The data does support that the benefits outweigh the risks for both of these doses in both of these age groups,” said the CDC’s Dr. Melinda Wharton, a member of the panel.

“I believe that this will provide families an important option” and may be particular­ly important for families who live in areas where coronaviru­s spread is increasing, said another panel member, Dr. Ofer Levy of Boston Children’s Hospital.

The FDA held up Moderna’s teen vaccine for months while it investigat­ed a rare side effect, heart inflammati­on. That’s mostly a risk for teen boys and young men, and also can occur with the Pfizer vaccine. Moderna got extra scrutiny because its shots are a far higher dose.

In their review, FDA scientists said there were no confirmed cases of the heart inflammati­on in Moderna’s kid studies. But experts say the studies may have had too few participan­ts for a rare side effect such as that to appear.

“That clearly needs to be watched closely going forward as we expand the use of the vaccine,” said Dr. Mark Sawyer, a panel member from the University of California, San Diego’s medical school.

As for other side effects, FDA officials said nothing worrisome was reported — mainly sore arms, headache and fatigue.

The FDA analysis concluded that two doses of Moderna are effective in preventing symptomati­c COVID-19 illness in teens and younger kids, with the levels of virus-fighting antibodies comparable to those developed in young adults.

Vaccine effectiven­ess was estimated at 93% for the teens and 77% for the younger children, according to the FDA analysis. However, the research was conducted when earlier versions of the coronaviru­s were causing most U.S. infections, before more contagious versions emerged. It’s also based on a limited number of COVID-19 cases, making the estimates a bit rough.

 ?? JENNY KANE/ASSOCIATED PRESS ?? A government advisory panel that met Tuesday to decide whether to recommend a second brand of COVID-19 vaccine for school-age children and teens has backed the Moderna shot.
JENNY KANE/ASSOCIATED PRESS A government advisory panel that met Tuesday to decide whether to recommend a second brand of COVID-19 vaccine for school-age children and teens has backed the Moderna shot.

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