The Latest: Johnson & Johnson single shot awaits approval

The Latest: Johnson & Johnson single shot awaits approval

SeattlePI.com

Published

WASHINGTON – An analysis by U.S. regulators say Johnson & Johnson’s single-dose vaccine protects against COVID-19.

The report Wednesday confirmed the vaccine is about 66% effective overall at preventing moderate to severe COVID-19.

On Friday, a panel of experts to the Food and Drug Administration will debate if the evidence is strong enough to recommend the vaccine. The FDA is expected to make a final decision within days.

If the FDA clears the J&J shot for U.S. use, it won’t boost vaccine supplies significantly right away. Only a few million doses are expected to be ready for shipping in the first week.

J&J tested its single-dose option in 44,000 people in the U.S., Latin America and South Africa. J&J previously announced the vaccine worked better in the U.S. -- 72% effective against moderate to severe COVID-19, compared with 66% in Latin America and 57% in South Africa.

Still, in every country it was highly effective against the most serious symptoms, and early study results showed no hospitalizations or deaths starting 28 days after vaccination.

___

THE VIRUS OUTBREAK:

— Johnson & Johnson single-dose COVID-19 shot poised for FDA decision

— U.S s tates scramble to catch up after weather disruptions, hope to administer more shots as vaccine supply increases

— UK to push at G-7 for global standard for vaccine passports

— A food fight erupts in France over serving meatless school lunches during pandemic

— Follow all of AP’s pandemic coverage at...

Full Article