FDA rethinks its strategy on future COVID vaccines

Illustration: Shoshana Gordon/Axios

An FDA advisory panel meeting tomorrow could start a reset of how the U.S. approaches its COVID-19 vaccine strategy.

Driving the news: The agency has sent signs they want to move from the on-the-fly response that's, at times, left the public confused to an annual vaccination schedule that more closely mirrors flu vaccines.

"It signals an idea of thinking for a longer-term horizon," Jason Schwartz, an associate professor at the Yale School of Public Health, who is not on the advisory panel, told Axios.

Yes, but: Experts on the Vaccines and Related Biological Products Advisory Committee, or VRBPAC, have serious questions about the reboot — and whether they have sufficient data to support it.

The big picture: CDC and FDA officials will present an update on the effectiveness and safety of the original and booster versions of the approved COVID vaccines. Pfizer, Moderna and Novavax will also present data on their shots.

Between the lines: One of the questions to watch is whether the committee continues backing bivalent booster doses, which are based on the original COVID strain and a later variant — or if the shots should only match the latest strain in circulation.

What to watch: Health experts say they'll also be closely watching any discussion that veers into new vaccine development.

Be smart: No matter what VRBPAC recommends and the FDA ultimately authorizes, officials are still essentially "flying blind," Michael Osterholm, director of the University of Minnesota's Center for Infectious Disease Research and Policy, told Axios.

https://www.axios.com/2023/01/25/america-rethinks-covid-strategy