The Novavax vaccine targets the same XBB.1.5 variant as the other two vaccines. That variant was the dominant one in the U.S. earlier this year when the FDA had to choose the makeup of this fall's ...

Novavax officials said they don't think the rate of myocarditis is any higher among trial participants than the general population, but FDA officials said it remains a question.

Most of the FDA’s Vaccines and Related Biological Products Advisory Committee voted “yes” in response to a question of whether the benefits of Novavax’s vaccine, given as a two-dose ...

The US Food and Drug Administration on Wednesday authorized Novavax’s Covid-19 vaccine for emergency use in adults. It is the fourth coronavirus vaccine available in the United States, and it ...

The Food and Drug Administration gave emergency use authorization on Tuesday to Novavax’s new Covid vaccine designed to target the coronavirus’ dominant XBB sublineage, which is fueling a ...

The new memos from the Food and Drug Administration show how the agency’s vaccine chief, Dr. Vinay Prasad, personally ...

If greenlighted by the FDA, Novavax's shots could be the first COVID-19 doses available in the U.S. based on a kind of "protein subunit" technology that has been used for decades in other routine ...

The FDA authorized the Covid-19 vaccine developed by Novavax, a small Maryland biotech firm, for people 18 and over.

In his weekend tweet, FDA's Makary referred to the Novavax vaccine as “a new product,” presumably because it had been updated to match last year's common coronavirus strain.

The Food and Drug Administration's independent panel of advisers has voted in favor of the FDA authorizing Novavax, a protein-based vaccine, which could soon be the fourth vaccine for COVID-19 ...

The FDA on Tuesday authorized Novavax’s updated Covid-19 vaccine, giving Americans seeking to update their protection against the SARS-CoV-2 virus another option.

Gaithersburg-based Novavax, Inc. announced its updated vaccine has received emergency use authorization from the FDA. (File photo) Associated Press // May 1, 2025 // ...