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FDA vaccine advisers vote to recommend booster doses of Covid-19 vaccine in people 65 and older and those at high risk

<i>Robyn Beck/AFP/Getty Images</i><br/>
AFP via Getty Images
Robyn Beck/AFP/Getty Images

By Maggie Fox, Jamie Gumbrecht and Jacqueline Howard, CNN

Vaccine advisers to the US Food and Drug Administration voted Friday to recommend emergency use authorization of a booster dose of Pfizer’s vaccine to people 65 and older and those at high risk of severe Covid-19 six months after they get their first two shots.

But the FDA’s Vaccines and Related Biological Products Advisory Committee rejected a broader application to approve booster doses of Pfizer’s vaccines for everyone 16 and older six months after they are fully vaccinated.

Members of the committee expressed doubts about the safety of a booster dose in younger adults and teens, and complained about the lack of data about the safety and long term efficacy of a booster dose.

Biden administration officials had previously announced a plan to begin administering booster doses to the general population during the week of September 20, irritating some members of the committee. They later noted that any action would be pending signoff from the FDA and US Centers for Disease Control.

Some of the advisers — a group of vaccine experts, immunologists, pediatricians, infectious disease specialists and public health experts — have said the process was rushed, and several members said during the meeting they wanted to see more data.

The group unanimously supported authorization for the more limited higher-risk group, and they informally advised the FDA to include health care workers or others at high risk of Covid-19 exposure in the EUA, too. The FDA will now craft its decision on Pfizer’s request, taking into account the committee’s guidance.

Dr. Archana Chatterjee, dean of the Chicago Medical School at Rosalind Franklin University, noted the lively discussion and adjustments during the meeting proved they are truly independent advisers.

“I think this should demonstrate to the public that the members of this committee are independent of the FDA, and that in fact we do bring our voices to the table when we are asked to serve on this committee,” she said.

Pfizer’s case for boosters

During the meeting, Dr. William Gruber, senior vice president of vaccine clinical research and development at Pfizer, said several studies indicate that people’s immunity can and does wane and that giving booster doses restores that immunity — sometimes to levels higher than seen at initial vaccination. He said people who got the boosters did not have any more side effects than seen after the first two doses.

And Gruber said while the two-dose Pfizer vaccine continues to protect well against severe infection, hospitalizations and deaths, there are hints that could change.

The company relied heavily on data from Israel, where vaccinated people started to get breakthrough infections. Israeli researchers earlier told the meeting that adding booster shots in Israel helped keep many people out of the hospital.

“The Israeli experience could portend the US Covid-19 future,” Gruber said. “Israel and the United States real world evidence suggests that vaccine efficacy against Covid-19 infection wanes approximately six to eight months following the second dose,” he added.

“In addition, recent US CDC data hint at reduced Covid-19 vaccine effectiveness over time against severe disease and hospitalization in the US,” he said. “This reduced vaccine effectiveness tracks with longer spans of time between two doses of vaccine and SARS coronavirus exposure.”

But FDA staff and advisers pushed back on the data available so far.

Dr. Phil Krause, deputy director of the FDA’s Office of Vaccines Research and Review, noted that Pfizer was using data that had not been reviewed by experts.

“One of the issues in this is that much of the data that’s been presented and being discussed today is not peer-reviewed and has not been reviewed by FDA,” Krause told the meeting of the Vaccines and Related Biological Products Advisory Committee.

Krause, along with another FDA vaccine official, Marion Gruber, signed a Lancet paper published earlier this week that argued it’s too soon to start giving people boosters.

Dr. Michael Kurilla, an infectious disease specialist at the National Center for Advancing Translational Sciences, noted that Pfizer’s studies relied heavily on measurements of antibodies, without looking at other important aspects of immune response.

“It’s a little disappointing that there’s been very little reporting of the cellular immune responses and an entire focus on the neutralizing antisera,” Kurilla said. “Which clearly for that population at high risk is absolutely essential, but for the broad population in terms of their protection, which seems to be holding up well over time — (that) should be because of adequate cellular immune responses but we have no indication of that.

“So it’s unclear that everyone needs to be boosted, other than a subset of the population that clearly would be at high risk for serious disease.”

Dr. Cody Meissner, a professor of pediatrics at Tufts University School of Medicine, said during the meeting he didn’t think boosters would significantly contribute to controlling the pandemic.

“It is very important that the main message that we still transmit is that we have got to get everyone two doses. Everyone has got the get the primary series,” he said. “This booster dose is not likely to make a big difference in the behavior of this pandemic.”

Pfizer received full approval for its vaccine from the FDA, so the request to add a booster dose is a supplement to that approval. Pfizer — and other researchers — say their studies show people develop strong immunity after two doses of vaccine, but that levels of antibodies start to drop after a few months.

The FDA noted in its briefing documents that Pfizer’s vaccine — as well as vaccines made by Moderna and Johnson & Johnson — still provide strong protection against severe disease, hospitalization and death, even if antibodies do wane over time.

After the FDA advisory committee makes its recommendation, the FDA makes the decision about whether to approve the booster dose.

“Today was an important step forward in providing better protection to Americans from COVID-19. We stand ready to provide booster shots to eligible Americans once the process concludes at the end of next week,” White House spokesman Kevin Munoz told CNN.

The CDC has scheduled a meeting of its vaccine advisers for September 22 and 23 — and CDC must give its stamp of approval for any booster doses to be officially given. In a letter sent Thursday and obtained by CNN, the CDC urged local and state health officials to wait to administer boosters until both agencies had signed off.

Third doses are already approved for certain immunocompromised people, but not for the general public.

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CNN’s Jacqueline Howard, Nadia Kounang and Phil Mattingly contributed to this report.

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