FDA OKs new COVID-19 shot from Novavax
The Food and Drug Administration cleared a COVID-19 vaccine from Novavax on Wednesday, giving U.S. adults a new option.
Novavax makes a more traditional type of protein vaccine that’s unlike the three other COVID-19 shots available for use in the U.S. The shots are already available in Europe and multiple other countries.
Nearly a quarter of American adults still haven’t gotten their primary vaccinations, and experts expect at least some of them to roll up their sleeves for Novavax’s more conventional option.
The Maryland company also hopes its shots can become a top booster choice in the U.S. and beyond. Tens of millions of Americans still need boosters that experts call critical for the best possible protection as the coronavirus continues to mutate.
For now, the FDA authorized Novavax’s initial two-dose series for people 18 and older.
“I encourage anyone who is eligible for, but has not yet received, a COVID-19 vaccine to consider doing so,†FDA Commissioner Dr. Robert Califf said in a statement.
Newfangled COVID-19 vaccines have left many people yearning for an old-school alternative. The one from Novavax could fit that bill.
Before shots are offered, the Centers for Disease Control and Prevention must recommend how they should be used. A decision from the CDC is expected next week.
Novavax Chief Executive Stanley Erck said he expected the U.S. to expand use of the vaccine beyond unvaccinated adults fairly quickly.
The FDA is already evaluating it for those as young as 12, Erck said. Novavax also has submitted data on booster doses, including “mix-and-match†use in people who’d earlier received Pfizer or Moderna vaccinations.
The Biden administration has bought 3.2 million Novavax doses so far, and Erck said vaccinations should begin later this month.
Sharon Bentley of Argyle, Texas, is a COVID-19 vaccine holdout. Bentley was hesitant about the first crop of vaccines. Then her husband volunteered for a Novavax trial, getting two doses and later a booster.
After her husband’s positive experience with a more tried-and-true technology, “that convinced me,†Bentley said, adding that she planned to tell some unvaccinated friends about the option too.
Determining which version of the coronavirus should be used to make COVID-19 vaccines and boosters is an exercise in educated guesswork.
The Novavax vaccine is made of copies of the spike protein that coats the coronavirus. They’re packaged into nanoparticles that, to the immune system, resemble a virus. Then an immune-boosting ingredient, or adjuvant, made from the bark of a South American tree is added. The adjuvant acts as a red flag to ensure the nanoparticles look suspicious enough to spark a strong immune response.
Protein vaccines have been used for years to prevent hepatitis B, shingles and other diseases. It’s a very different technology from the dominant Pfizer and Moderna COVID-19 vaccines that use mRNA to deliver genetic instructions for the body to produce its own copies of the spike protein. The lesser-used Johnson & Johnson option uses a harmless cold virus to deliver spike-making instructions.
Like the other vaccines used in the U.S., the Novavax shots have proved highly effective at preventing COVID-19’s most severe outcomes. Typical vaccine reactions were mild, including arm pain and fatigue. But the FDA did warn about the possibility of a rare risk, heart inflammation, that also has been seen with the Pfizer and Moderna vaccines.
The Novavax vaccine was tested long before the Omicron variant struck. But last month, the company released data showing a booster dose promised a strong immune response even against Omicron’s newest subvariants — preliminary evidence that several of the FDA’s scientific advisors called compelling.
Americans may soon get a new COVID-19 vaccine option — a more traditional kind of shot known as a protein vaccine.
Still, U.S. regulators are planning for a fall booster campaign that includes Pfizer and Moderna shots designed to better target the BA.4 and BA.5 Omicron subvariants. Novavax also has begun testing updated shots, and Erck said the company could have updated doses available late in the year.
European regulators recently cleared the Novavax vaccine to be used in adolescents as young as age 12, and several countries have authorized booster doses of its original vaccine.
Manufacturing difficulties held up the vaccine, although Erck said those have been resolved and Novavax can meet global demand. Much of the company’s vaccine, including doses for the U.S., are being produced by the Serum Institute of India, the world’s largest vaccine manufacturer.
