News from the FDA/CDC

Johnson & Johnson requests FDA approval for vaccine booster doses


 

Johnson & Johnson asked the Food and Drug Administration (FDA) on Tuesday to authorize an extra dose of its COVID-19 vaccine as a booster shot.

The company said it filed a request for people ages 18 and older who have received the one-shot vaccine. Johnson & Johnson submitted data for several different booster intervals -- ranging from 2 months to 6 months -- but didn’t formally recommend one to the FDA, The Associated Press reported.

“We’re describing the data to them,” Mathai Mammen, MD, head of global research and development for Janssen, the company’s vaccine division, told CNN.

“The process is not that we asked for a very specific interval -- we’re providing them data and we’re going to be presenting to the committee,” he said. “They’ll take all that into consideration when they ultimately decide on an appropriate interval.”

The FDA’s independent vaccine advisory committee meets next week to review data on booster shots from both Johnson & Johnson and Moderna. It’s the first step in the review process, which then requires approval from leaders at the FDA and Centers for Disease Control and Prevention. If both agencies authorize the extra shots, Americans could receive boosters from Johnson & Johnson and Moderna later this month, the AP reported.

Johnson & Johnson previously released data that showed the vaccine remains highly effective against COVID-19 at least 5 months after vaccination, with 81% efficacy against hospitalizations in the United States.

Two weeks ago, the company reported that a booster dose at 2 months or 6 months further lifted immunity, with a booster at 2 months providing 94% protection against moderate and severe COVID-19. The company said the 6-month booster raised antibodies by 12 times but didn’t release additional data at that time.

In September, the FDA authorized booster shots of the Pfizer vaccine for ages 65 and older, those who live in long-term care facilities, and those with higher risks for contracting COVID-19. The Biden administration is supporting a booster campaign to address potential waning vaccine immunity and remaining surges of the more contagious Delta variant, the AP reported.

A version of this article first appeared on WebMD.com.

Recommended Reading

Booster shot back-and-forth creates uncertainty, confusion
MDedge Internal Medicine
CVST after COVID-19 vaccine: New data confirm high mortality rate
MDedge Internal Medicine
Worried parents scramble to vaccinate kids despite FDA guidance
MDedge Internal Medicine
Drug cocktail significantly reduced severe COVID, death in outpatients
MDedge Internal Medicine
More U.S. adults vaccinated, but partisan divide remains: Survey
MDedge Internal Medicine
Should clinicians recommend vitamin D for psychiatric patients during COVID-19?
MDedge Internal Medicine
Antibody cocktail reduces chance of developing COVID
MDedge Internal Medicine
Pfizer COVID vaccine antibodies may disappear in 7 months, study says
MDedge Internal Medicine
COVID-19: Two more cases of mucosal skin ulcers reported in male teens
MDedge Internal Medicine
Vaccine holdouts embrace COVID antibody treatment, mystifying doctors
MDedge Internal Medicine