AstraZeneca prioritizes US for RSV drug amid surge in cases
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[November 11, 2023]
By Patrick Wingrove and Maggie Fick
NEW YORK (Reuters) - AstraZeneca on Friday said it was prioritizing the
U.S. market for additional doses of its respiratory syncytial virus
(RSV) drug Beyfortus, which was approved in July to prevent the disease
in infants and toddlers, as a surge of cases is outpacing supply.
AstraZeneca CEO Pascal Soriot in an interview at the Reuters office in
New York said the U.S. Centers for Disease Control and Prevention (CDC)
had been asking for more of the antibody therapy that was co-developed
with French drugmaker Sanofi.
“We’ve had to deliver what is needed (for the U.S.) and next year the
volume suddenly will go up quite a bit,” Soriot said, noting that the
British drugmaker was seeing a surge in demand for the medicine
"everywhere."
The CDC was did not immediately respond to a request for comment.
Sanofi on Oct. 20 said it was seeing an "unprecedented level" of demand
for Beyfortus. Three days later, the CDC issued an alert saying there
was a limited supply of the drug, and advised physicians to prioritize
those under 6 months of age or with underlying health conditions.
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CEO of AstraZeneca Pascal Soriot speaks at an announcement at
AstraZeneca in Mississauga Ontario, Canada February 27, 2023.
REUTERS/Carlos Osorio/File Photo
RSV cases in the U.S. began a sharp
upward trend in the middle of October and were at the highest level
since January last winter with 4,952 cases detected through testing
in the week ended Nov. 4, according to the CDC website. The website
also shows an increase in hospitalizations largely among children
ages 4 years and under during the same period.
RSV is the top cause of hospitalization among infants, leading to
around 1% to 3% of children under 12 months of age being
hospitalized in the United States each year, according to the
American Academy of Pediatrics.
The U.S. last year saw a surge of children under age 5 being
hospitalized for respiratory viruses, including RSV.
Before the approval of Beyfortus, Swedish Orphan Biovitrum had the
only approved preventive therapy in the United States for high-risk
infants, called Synagis.
(Reporting by Patrick Wingrove; Editing by Caroline Humer and Bill
Berkrot)
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