J&J applies for emergency approval for one-shot vaccine

world
J&Amp;J Applies For Emergency Approval For One-Shot Vaccine
Share this article

By Associated Press Reporters

Johnson & Johnson has asked US regulators to clear the world’s first single-dose coronavirus vaccine, an easier-to-use option that could boost scarce supplies.

Preliminary results from a massive study of 44,000 people in the US, Latin America and South Africa showed the jab was safe and offered strong protection against moderate to severe Covid-19.

Advertisement

It did not appear quite as strong as two-dose competitors made by Pfizer and Moderna.


Overall, the single-dose vaccine was 66% effective at preventing moderate to severe Covid-19 but it was 85% protective against the most serious symptoms — and starting 28 days after their shot, researchers found no one who got the vaccine needed hospitalisation or died.

Johnson & Johnson filed an application with the Food and Drug Administration (FDA) on Thursday.

Advertisement

An FDA panel will meet later this month and pore over the results.


 

Advertisement

Dr Peter Marks, FDA’s vaccine chief, has cautioned against making comparisons before the evidence is all in.

“With so much need to get this pandemic under control, I think we can’t ignore any tool in the tool chest,” he told the American Medical Association last week.

“We will have to do our best to try to make sure that we find the populations that benefit the most from each of these vaccines and deploy them in a very thoughtful manner.”

J&J also is studying a two-dose version of its vaccine, but results will not be available for several more months.

Advertisement

Read More

Message submitting... Thank you for waiting.

Want us to email you top stories each lunch time?

Download our Apps
© BreakingNews.ie 2024, developed by Square1 and powered by PublisherPlus.com