Sanofi, GSK variant-specific COVID shot found effective against Omicron
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[June 24, 2022]
By Natalie Grover
PARIS/LONDON (Reuters) -Late-stage data on
an experimental COVID-19 vaccine from Sanofi and GSK has showed the shot
confers protection against the Omicron variant of the virus, the
companies said on Friday.
The so-called bivalent vaccine targets the Beta variant - first
identified in South Africa - as well as the original Wuhan strain of the
virus.
In a trial involving 13,000 adults, the vaccine demonstrated an efficacy
rate of 64.7% against symptomatic COVID, and 72% efficacy against
infections specifically caused by the Omicron variant.
When used in people who previously had COVID, the results were stronger.
The vaccine generated an efficacy rate of 75.1% against symptomatic
COVID and 93.2% in Omicron-confirmed symptomatic cases, the companies
said.
"Sanofi-GSK’s vaccine is the first candidate to demonstrate efficacy in
a placebo-controlled trial in an environment of high Omicron variant
circulation," Sanofi said in a statement.
Sanofi's Paris-listed shares and GSK's London-listed shares were both up
more than 1% in morning trading.
Earlier this month, the bivalent vaccine showed potential in two trials
to protect against the virus' main variants of concern - the Omicron
BA.1 and BA.2 strains - when used as a booster shot.
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A logo on the Sanofi exhibition space at the Viva Technology
conference dedicated to innovation and startups at Porte de
Versailles exhibition center in Paris, France June 15, 2022.
REUTERS/Benoit Tessier
Sanofi and GSK, two of the world's biggest vaccine makers, are
hoping to gain a foothold in the market for next-generation
variant-focused COVID shots, after falling behind competitors
including Moderna, AstraZeneca and Pfizer-BioNTech, in the original
race to contain the pandemic.
The new data supporting the bivalent vaccine will be submitted to
regulatory authorities with the hope of making the shot available
later this year, the companies said on Friday.
Sanofi and GSK's original COVID vaccine is already under review by
the European Medicines Agency.
The companies have bet that this bivalent vaccine moulded on the
now-supplanted Beta variant will confer broad protection against
future viral strains on the basis that Beta expresses similar
mutations across multiple variants of concern, including Omicron.
(Reporting by Tassilo Hummel in Paris nd Natalie Grover in London;
Editing by Clarence Fernandez and Edmund Blair)
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