WASHINGTON, Feb 28, 2021 (BSS/AFP) – The United States on Saturday
authorized Johnson & Johnson’s Covid vaccine for emergency use, giving the
nation a third shot to battle the outbreak that has killed more than 500,000
Americans.
The single-shot vaccine is highly effective in preventing severe Covid-19,
including against newer variants, the Food and Drug Administration (FDA) said
before giving it a green light.
“This is exciting news for all Americans, and an encouraging development in
our efforts to bring an end to the crisis,” US President Joe Biden said in a
statement.
But he urged Americans to remain vigilant with anti-virus curbs such as
social distancing, warning that new variants of the virus still posed a
threat.
“But we cannot let our guard down now or assume that victory is
inevitable,” he said.
A third vaccine is seen as a vital means to ramp up the immunization rate
in the United States, where more than 500,000 people have lost their lives to
the coronavirus.
In large clinical trials, the J&J vaccine’s efficacy against severe disease
was 85.9 percent in the United States, 81.7 percent in South Africa, and 87.6
percent in Brazil.
Overall, among 39,321 participants across all regions, the efficacy against
severe Covid-19 was 85.4 percent, but it fell to 66.1 percent when including
moderate forms of the disease.
Crucially, analyses of various demographic groups revealed no marked
differences across age, race, or people with underlying conditions.
– 100 million doses by June –
The J&J vaccine is the third to be greenlighted in the United States after
Pfizer’s and Moderna’s were provisionally approved in December.
Over 65 million people in America have so far received at least one shot of
either the Pfizer or Moderna vaccines — but unlike those, the J&J vaccine
requires just one dose, and is stored at fridge temperatures, offering
logistical and practical advantages.
The J&J shot appears less protective than Pfizer and Moderna’s two-shot
regimens, which both have an efficacy of around 95 percent against all forms
of Covid-19 from the classic coronavirus strain.
All three have been shown to fully protect against hospitalizations and
death, however.
Nirav Shah, director of the Maine Center for Disease Control and
Prevention, told The Washington Post the two earlier vaccines were tested
months before the emergence of “variants of concern” that could affect the
efficacy, meaning the Pfizer and Moderna results were not an “apples to
apples” comparison with the J&J shot.
There was a hint, based on preliminary data, that the J&J vaccine might be
effective against asymptomatic infection — though the company said it needs
to do more research.
The company has announced it aims to deliver 20 million doses by the end of
March, with 100 million by June — though the US is pushing to expedite that
timeline.
The J&J vaccine uses a common-cold causing adenovirus, which has been
genetically modified so that it can’t replicate, to carry the gene for a key
protein of the coronavirus into human cells.