UK rolls out Astra/Oxford COVID vaccine after world-first approval
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[December 31, 2020]
By Alistair Smout and Paul Sandle
LONDON (Reuters) - Britain on Wednesday
became the first country in the world to approve a coronavirus vaccine
developed by Oxford University and AstraZeneca, hoping that rapid action
would help it stem a surge of infections driven by a highly contagious
variant of the virus.
Boris Johnson’s government, which has already ordered 100 million doses
of the vaccine, has jumped ahead of other Western countries with its
vaccination programme.
It was the first to approve a shot developed by Pfizer of the United
States and Germany's BioNTech, with the result that hundreds of
thousands of people were vaccinated in Britain before European Union
countries and the United States even began administering it this month.
The AstraZeneca/Oxford shot, unlikely to be approved for some time by EU
or U.S. regulators, will start being administered on Monday, beginning
with those most at risk from COVID-19.
While the approval by the UK Medicines and Healthcare products
Regulatory Agency (MHRA) is a vindication for a shot seen as essential
for mass immunisations in the developing world as well as in Britain, it
does not eliminate questions about trial data that make it unlikely to
be approved so rapidly in the European Union or the United States.
Uncertainty has swirled over the most effective dosing pattern for the
AstraZeneca/Oxford vaccine since it released data last month showing a
90% success rate for a half-dose followed by a full dose, but only 62% -
still usually more than enough for regulators - for two full doses.
The MHRA said that the results for the half-dose regimen had not been
borne out by analysis. Instead, it approved the regimen of two full
doses.
An official involved in the MHRA decision, said that the vaccine's
effectiveness had risen when the doses were given three months apart.
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Vials with a sticker reading, "COVID-19 / Coronavirus vaccine /
Injection only" and a medical syringe are seen in front of a
displayed AstraZeneca logo in this illustration taken October 31,
2020. REUTERS/Dado Ruvic/Illustration/File Photo
"Effectiveness was high, up to 80%, when there was a three- month
interval between first and second doses, which is the reason for our
recommendation," Munir Pirmohamed, Chair of the Commission on Human
medicines expert Working Group on COVID-19 vaccines, told reporters.
Hancock said hundreds of thousands of doses would be available to
administer next week in Britain.
"The NHS (National Health Service) will be able to deliver these
shots into people's arms at the speed at which it can be
manufactured," Health Secretary Matt Hancock told Sky News.
"I am also now, with this approval this morning, highly confident
that we can get enough vulnerable people vaccinated by the spring
that we can now see our route out of this pandemic."
Crucially for countries with relatively basic health infrastructure,
the AstraZeneca/Oxford vaccine can be stored and transported under
normal refrigeration, rather than supercooled to -70 degrees Celsius
(-94 Fahrenheit).
India is keen to start administering the new shot next month; Serum
Institute of India (SII), the world's biggest producer of vaccines,
has already made about 50 million doses. Chile is also interested.
(Reporting by Alistair Smout and Paul Sandle in London, additional
reporting by Pushkala Aripaka in Bengaluru, Kate Kelland in London,
John Miller in Zurich, Emilio Parodi in Milan; editing by Guy
Faulconbridge and Kevin Liffey)
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