J&J’s one-dose COVID-19 vaccine SHOULD get FDA authorization, experts vote


BREAKING NEWS: Johnson & Johnson’s one-dose COVID-19 vaccine SHOULD get FDA authorization, expert panel votes: Advisors give unanimous ‘yes’ for America’s third shot

  • FDA’s advisory committee recommended that the FDA give emergency approval for J&J’s shot on Friday 
  • The shot was 66% effective at preventing mild to moderate infection in trials globally, and 72% effective in the US 
  • It prevented 100% of deaths from COVID-19 and virtually all hospitalizations 
  • J&J’s data on elderly people was thin, so its shot may not be authorized for Americans over 75 
  • J&J said it can only provide three to four million doses upon authorization, which could come Saturday
  • But by the end of June J&J it says it will supply 100 million doses 
  • Together with Pfizer and Moderna doses, that would give the US enough doses to fully vaccinate every adult in the country  

America is one step closer to having a one-dose COVID-19 vaccine after an expert panel voted that the Food and Drug Administration (FDA) should authorize the shot on Friday.  

The panel voted unanimously – 21 to zero – in favor of the vaccine, which was found to be 66 percent effective in trials in the US, Latin America, and South Africa, with efficacy reaching 72 percent among Americans. 

It sets the stage for the unleashing of millions more doses across the country next week. 

With 100 million doses of the single-shot expected by the end of June, the additional doses could boost the US stockpile enough to have enough vaccine to inoculate every American. 

But Johnson & Johnson admitted earlier this month that only three or four million doses will be available immediately upon authorization.  

The FDA is likely to authorize the vaccine for emergency use within a day or so, making it the third available in the United States, and the only one that requires just one shot.

Johnson & Johnson’s vaccine was 100 percent effective at preventing COVID-19 deaths in trials and prevented 66 percent of mild to moderate infections. In tests in South Africa, where the worrisome B1351 variant is dominant, the vaccine was 64 percent effective.   

FDA advisors on Friday voted that the FDA should authorize J&J’s one-dose COVID-19 vaccine 

The panel was particularly glad that vaccine can be easily stored, at just refrigerator temperatures of between 35.6 and 46.4F. 

That is ‘very practical for rural areas in the US and across the world,’ said one of the panelists, Dr Cody Meisner.  

J&J’s vaccine also had a low rate of side effects in a 44,000-person trial. Sixty-one percent of participants had some reaction, but just 2.3 percent were considered severe.   

Most people who had side effects had nausea, fatigue, headaches, body aches or fevers. 

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The vaccine was 66 percent effective at preventing moderate-to-severe cases of COVID-19 compared with a placebo in the context of trials in North America, South America and South Africa. 

The effectiveness of the one-dose vaccine varied over time and location. 

In the United States, the effectiveness was 74 percent at 14 days and 72 percent two weeks later, while the shot was 64 percent effective at stopping moderate-to-severe COVID-19 after 28 days in South Africa, where a worrying new variant has swept across the country.

The vaccine was 100 percent effective at preventing hospitalizations 28 days after vaccination and there were no COVID-19 deaths among those who received the shot.

The J&J vaccine can be stored in normal refrigerator temperatures, making distribution easier than that of the Pfizer Inc/BioNTech SE and Moderna Inc vaccines that use mRNA technology and must be shipped and stored frozen.

J&J’s vaccine uses a common cold virus known as adenovirus type 26 to introduce coronavirus proteins into cells in the body and trigger an immune response.

Three to four million doses of the vaccine are expected to be rolled out next week.

Read more at DailyMail.co.uk