Johnson & Johnson's long-awaited one-shot vaccine WORKS: One jab prevents 72% of COVID-19 in the US and is 66% effective in Brazil and 57% effective in South Africa where 'super-covid' variants are spreading

 Johnson & Johnson on Friday said its single-dose vaccine was 72 percent effective in preventing COVID-19 in the US, but a lower rate of 66 percent was observed globally in the large trial conducted across three continents and against multiple variants.

The US has a $1 billion contract with Johnson & Johnson (J&J) for 100 million doses, pending the green light from the Food and Drug Administration (FDA). The firm has said it is on track to provide the doses by June. 

J&J said Friday it will file for emergency use authorization from the FDA 'inside of a week,' according to VOA.

In the trial of nearly 44,000 volunteers, the level of protection against moderate and severe COVID-19 was 66 percent in Latin America and just 57 percent in South Africa, where a particularly worrying variant of the novel coronavirus is circulating.

Those results compare to the high bar set by two authorized vaccines from Pfizer and partner BioNTech and Moderna, whose two-dose shots were around 95 percent effective in preventing symptomatic illness.  

Those trials, however, were conducted mainly in the United States and before the broad spread of new variants now under the spotlight.

Brazil's variant is triggering massive outbreaks and reinfections there, and one case has been reported in the US. 

Dr Anthony Fauci warned that the South African variant was most concerning to him because it has mutations - shared by the Brazilian variant - that could make vaccines less effective. 

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A single dose of Johnson & Johnson's vaccine prevents 72% of COVID-19 cases in the US but was only 66% effective in  Brazil and 57% effective in South Africa where variants carrying mutations that may make vaccines less effective are common

J&J's main study goal was the prevention of moderate to severe COVID-19, and the vaccine was 85 percent effective in stopping severe disease and preventing hospitalization across all geographies and against multiple variants 28 days after immunization.

That level of prevention 'will potentially protect hundreds of millions of people from serious and fatal outcomes of COVID-19,' Dr Paul Stoffels, J&J's chief scientific officer, said in a statement.

The company plans to seek emergency use authorization from the U.S. Food and Drug Administration next week.

Public health officials have been counting on the J&J vaccine to increase much-needed supply and simplify the US immunization campaign.

Unlike the Pfizer/BioNTech and Moderna vaccines, J&J's does not require a second shot weeks after the first or need to be kept frozen, making it a strong candidate for use in parts of the world with weak transportation infrastructure and insufficient cold storage facilities.

SOUTH AFRICA'S VARIANT MAKES J&J'S VACCINE WEAKER - BUT IT STILL PREVENTED NEARLY 90% OF SEVERE INFECTIONS

Several studies have emerged this month showing that a South African variant of the coronavirus has mutated in areas of the virus that are key targets of vaccines, reducing their efficacy.

'What we are learning is there is different efficacy in different parts of the world,' Stoffels said in a telephone interview.

Importantly, though, in a sub-study of 6,000 volunteers in South Africa, Stoffels said, the J&J vaccine was 89 percent effective at preventing severe disease. Ninety-five percent of cases in the South Africa portion of the trial were infections with the South African variant.

A mid-stage trial of a Novavax Inc coronavirus vaccine in South Africa also showed lower efficacy in the country. It proved to be 60 percent effective among volunteers who didn't have HIV. In a separate, late-stage trial in the UK, the vaccine was 89.3% effective.

In the J&J trial, which was conducted in eight countries, 44 percent of participants were from the United States, 41 percent were from Central and South America and 15 percent were from South Africa. Slightly more than a third of the volunteers were over age 60.

There were no serious adverse events among those who received the shot, the company said. Full results will be published in a peer-reviewed journal.

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.

The Pfizer/BioNTech and Moderna vaccines use a new technology called messenger RNA (mRNA) that requires it to be stored in a freezer.

VACCINES FROM J&J AND NOVAVAX COULD SPEED THE SLOW US ROLLOUT TOWARD BIDEN'S GOAL OF 100M SHOTS IN 100 DAYS 

The news of another safe and effective vaccine comes as the United States has surpassed 430,000 COVID-19 deaths and with hospitals in many states still struggling to keep up with patients despite recent declines in new infections.

Concerns about fresh surges in the United States have also grown due to the presence of a more contagious coronavirus variant first discovered in the UK and news of the arrival of the South African variant on Thursday in South Carolina, as well as the  Brazilian variant in Minnesota, announced on Monday. 

The US vaccination program got off to a slow start in December and has accelerated to around one  million shots per day nationwide.

President Joe Biden has promised that at least 100 million shots will be administered in his first 100 days in office, but concerns about supply disruptions have added uncertainty to that target.

The United States has an agreement to buy 100 million doses of J&J's vaccine for $1 billion. 

The company said in a statement the vaccine would be ready immediately upon emergency approval but Stoffels declined to specify how many doses. The government also has the option of purchasing an additional 200 million doses.

J&J has said it plans to deliver 1 billion doses in 2021 and will produce the vaccine in the United States, Europe, South Africa and India.

US trial results for the vaccine from AstraZeneca Plc and Oxford University are expected in early February, opening up the possibility of a fourth vaccine option. It has already been approved in the UK, Europe and many countries based on results of a separate tria

Novavax is also discussing with the FDA whether its data is sufficient to apply for emergency use authorization.

J&J is studying the effects of its vaccine given in two doses at two months apart, but results of that trial won't be available until this summer, Stoffels said.