The Atlanta Journal-Constitution

Pfizer asks FDA to allow all adults to get a booster

Company submitting early results of a study to make its case.

- By Lauran Neergaard

Pfizer asked U.S. regulators Tuesday to allow boosters of its COVID-19 vaccine for anyone 18 or older, a step that comes amid concern about increased spread of the coronaviru­s with holiday travel and gatherings.

Older Americans and other groups particular­ly vulnerable to the virus have had access to a third dose of the Pfizer and Biontech vaccine since September. But the Food and Drug Administra­tion has said it would move quickly to expand boosters to younger ages if warranted.

Pfizer is submitting early results of a booster study in 10,000 people to make its case that it’s time to further expand the booster campaign.

While all three vaccines used in the U.S. continue to offer strong protection against severe COVID-19 illness and death, the shots’ effectiven­ess against milder infection can wane over time. Pfizer’s new study concluded a booster could restore protection against symptomati­c infection to nearly 96%, even as the extra-contagious delta variant was surging. Side effects were similar to those seen with the company’s first two shots.

A median of 11 months after their last Pfizer vaccinatio­n, trial participan­ts were given either a third dose or a dummy shot. Researcher­s tracked any infections that occurred at least a week later, and so far have counted five cases of symptomati­c COVID-19 among booster recipients compared to 109 cases among people who got dummy shots.

The Biden administra­tion had originally envisioned boosters for all adults, but faced a stinging setback in September when the

FDA’S scientific advisers rejected extra Pfizer doses for everyone.

Still, under today’s policies about 2 of every 3 vaccinated adults is expected to qualify within the next few months .

The current rules: People who initially received Pfizer or Moderna vaccinatio­ns are eligible for a booster six months later if they’re 65 or older, or are at high risk of COVID-19 because of underlying health problems or their job or living conditions. Because the single-dose Johnson & Johnson vaccine hasn’t proven as effective as its two-dose competitor­s, any J&J recipient can get a booster at least two months later. And regardless of the initial vaccinatio­n, the U.S. has cleared getting a booster of a different company’s vaccine, what’s called mixing and matching.

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