FDA signs off on updated Covid-19 vaccines that target circulating variants
Sep 11, 2023, 11:59 AM | Updated: 1:15 pm
(Lea Suzuki/San Francisco Chronicle/AP/FILE)
(CNN) — The US Food and Drug Administration gave the green light Monday to updated Covid-19 vaccine booster shots from Moderna and Pfizer/BioNTech amid rising cases and hospitalizations.
Both vaccine manufacturers have said testing shows that their vaccines are effective against EG.5, the currently dominant strain in the United States.
The Advisory Committee on Immunization Practices, a group of independent experts that advises the US Centers for Disease Control and Prevention on its vaccination decisions, will now weigh the safety and effectiveness of the updated vaccines and make recommendations for their use. After the CDC director signs off on those recommendations, the vaccines can be administered.
The advisory group is scheduled to meet to discuss Covid-19 vaccines Tuesday, meaning the vaccines could become available within just a few days at certain pharmacies and doctor’s offices.
Health officials are urging people to get vaccinated as soon as the shots are available. They’re debuting amid a late summer rise in Covid-19 hospitalizations in the United States and growing concerns about the effects that the triple threat of respiratory viruses – coronavirus, flu and respiratory syncytial virus – may have this fall and winter season.
“Vaccination remains critical to public health and continued protection against serious consequences of COVID-19, including hospitalization and death,” Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, said in a news release Monday. “The public can be assured that these updated vaccines have met the agency’s rigorous scientific standards for safety, effectiveness, and manufacturing quality. We very much encourage those who are eligible to consider getting vaccinated.”
Experts have expressed concerns about the impacts the triple threat of viral illnesses will have this fall. The CDC has already warned that RSV levels are starting to pick up in the South, doubling between late July and late August. RSV cases are also beginning to slightly increase in parts of the West and Midwest, according to the CDC. However, the overall uptick is small relative to recent season peaks.
The new FDA decision “comes at a time when COVID-19 cases are once again climbing. Now, most people 6 months or older in the U.S. are eligible to receive this season’s COVID-19 vaccine, even if they have never been vaccinated against COVID-19 before,” Albert Bourla, chairman and chief executive officer at Pfizer, said in a news release.
The updated vaccines are approved for people 12 and older and are authorized under emergency use for individuals 6 months through 11 years old. As part of the FDA’s update, the bivalent Moderna and Pfizer/BioNTech Covid-19 vaccines are no longer authorized for use in the United States.
According to the FDA, babies and young children ages 6 months through 4 years who have not been vaccinated against the coronavirus are eligible to receive three doses of the updated Pfizer/BioNTech shot or two doses of the updated Moderna booster.
For those in that age group who have been vaccinated, the number and timing of doses depends on the doses they’ve previously received.
According to the FDA, people 5 and older are eligible to receive a single dose of the updated vaccines at least two months since their last dose of any Covid-19 shot, regardless of previous vaccination.
The mRNA vaccines have been updated to teach the body to fight the XBB.1.5 Omicron subvariant of the coronavirus and other closely related strains that are circulating.
“With today’s decision, an updated vaccine will shortly become available that helps address multiple Omicron XBB-related sublineages, which currently account for the vast majority of COVID-19 cases globally,” Dr. Ugur Sahin, CEO and co-founder of BioNTech, said in a news release.
“Studies about confirmed viral infections suggest that COVID-19 adopts a seasonal pattern with peaks in fall and winter, similar to other respiratory viruses,” Sahin said. “Our goal is to provide people worldwide with COVID-19 vaccines that are adapted to circulating virus variants or sublineages.”
The updated Covid-19 vaccine, given in a single dose, “will be available to everyone who needs it, and it most likely will be available at no cost for the foreseeable future,” said Lori Tremmel Freeman, chief executive officer of the National Association of County and City Health Officials.
The FDA has not authorized an updated Covid-19 vaccine from Novavax, but the company said it expects its protein-based vaccine to be available this month.
Under the Affordable Care Act, most insurance plans are covering the full cost of vaccines, without co-pays. So most insured people will be able to get the updated Covid-19 vaccine at their doctor’s offices or pharmacies, such as CVS or Walgreens, at no cost.
People who are uninsured or underinsured may access the updated vaccine for free through the CDC’s Bridge Access Program. The new government program allows the CDC to purchase and distribute Covid-19 vaccines and allocate them through its network of state and local health departments. Vaccines for federally qualified health centers as well as certain pharmacy chains will be supported through both government and manufacturer-supplied resources.
The Bridge Access Program is temporary. According to the CDC’s website, free vaccines through the program will not be available after December 2024.
Although vaccines were previously provided for free by the government, this is the first time they will be provided through the commercial market. During a Pfizer investor call in October, officials said a potential US list price for the updated vaccine could be between $110 and $130 per single dose for adults.
CNN’s Brenda Goodman contributed to this report.
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