AstraZeneca confident new COVID antibody protects against known variants
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[April 19, 2023]
By Maggie Fick
BARCELONA (Reuters) - AstraZeneca is confident that its new version of
COVID-19 antibody treatment could protect immunocompromised patients
against all known virus variants, its vaccines head said.
Laboratory studies show the antibody, called AZD3152, neutralizes all
known variants of COVID-19 and AstraZeneca has support from regulators
to make the treatment available by the end of this year, Iskra Reic said
in an interview on Tuesday.
AstraZeneca plans, pending more positive data and regulatory approval,
to make the antibody available by the end of 2023.
These types of therapies are most needed for people with compromised
immune systems, either because of underlying conditions or because they
are undergoing immune suppressing treatments. They account for nearly 2%
of the global population.
In January, the U.S. health regulator withdrew its emergency use
authorization for AstraZeneca's original COVID-19 antibody cocktail
Evusheld, as new dominant variants made it obsolete.
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A vial labelled "AstraZeneca COVID-19
Vaccine" is seen in this illustration taken January 16, 2022.
REUTERS/Dado Ruvic/Illustration/File Photo
The U.S. Food and Drug
Administration's (FDA) decision resonated with concerns raised by
Europe's health regulator.
AstraZeneca's AZD3152, it new COVID-19 antibody, was acquired
through a $157 million deal last year with British biotech start-up
RQ Bio.
The British drugmaker will likely make future investments like its
current partnerships with RQ Bio but did not have any deals to
announce, said Reic, a longtime AstraZeneca executive who has led
the company's vaccines and immune therapies unit since it was formed
in late 2021, during the pandemic.
Last year, the unit made $4.8 billion in revenues. However, demand
for COVID-19 vaccines have dramatically declined with competition
from mRNA vaccines and given many countries already have an
oversupply of COVID-19 shots.
(Reporting by Maggie Fick in Barcelona; Additional reporting by
Natalie Grover in London; Editing by Alexander Smith)
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