US FDA approves Sanofi-AstraZeneca's preventive RSV therapy for babies
Send a link to a friend
[July 18, 2023]
(Reuters) -The U.S. Food and Drug Administration (FDA) said on
Monday it had approved Sanofi and partner AstraZeneca's antibody therapy
to prevent respiratory syncytial virus (RSV) in infants and toddlers.
The therapy, branded Beyfortus, was approved for preventing lower
respiratory tract disease in infants born during or entering their first
RSV season, and in children up to 24 months of age who remain vulnerable
to severe RSV disease through their second such season.
The companies plan to make Beyfortus available in the United States
ahead of the upcoming RSV season, Sanofi said, adding that it plans to
share more information about the therapy's price closer to the season.
RSV is a leading cause of hospitalizations in infants and so far Swedish
Orphan Biovitrum's treatment, Synagis, was the only approved preventive
therapy in the United States for high-risk infants.
Unlike Synagis, which is given as monthly injections, Beyfortus is a
long-acting therapy that can be given once every season to prevent
infection regardless of additional medical conditions in infants.
[to top of second column]
|
Signage is seen outside of the Food and
Drug Administration (FDA) headquarters in White Oak, Maryland, U.S.,
August 29, 2020. REUTERS/Andrew Kelly/File Photo
According to the American Academy of
Pediatrics, around 1% to 3% of children under 12 months of age in
the country are hospitalized each year due to RSV.
Beyfortus' approval comes more than a month after the agency's panel
of outside advisers voted in favor of the therapy's use.
The approval was based on the therapy's three studies, including a
late-stage trial, which showed a 74.5% reduction in incidence of
lower respiratory tract infections that require medical care in
infants.
The therapy comes with warnings and precautions about serious
hypersensitivity reactions, and should be given with caution to
infants and children with clinically significant bleeding disorders,
the FDA said.
(Reporting by Bhanvi Satija and Raghav Mahobe in Bengaluru; Editing
by Shinjini Ganguli and Maju Samuel)
[© 2023 Thomson Reuters. All rights
reserved.]This material may not be published,
broadcast, rewritten or redistributed.
Thompson Reuters is solely responsible for this content. |