US FDA approves Biogen-Sage Therapeutics pill for postpartum depression
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[August 05, 2023]
(Reuters) -The U.S. Food and Drug Administration (FDA) on Friday
approved Biogen and Sage Therapeutics' oral pill to treat postpartum
depression (PPD) in adults.
The companies had sought the FDA's approval for the drug, Zurzuvae, to
treat major depressive disorder (MDD), or clinical depression, as well
as postpartum depression, which affect millions of people.
PPD severely affects a woman's ability to return to normal functioning,
while also potentially affecting the mother's relationship with her
child.
"Zurzuvae is expected to launch and be commercially available in the
fourth quarter of 2023 shortly following scheduling as a controlled
substance by the U.S. Drug Enforcement Administration, which is
anticipated to occur within 90 days," Sage Therapeutics and Biogen said
in a statement.
The statement said the FDA issued a Complete Response Letter for the New
Drug Application for Zurzuvae in the treatment of adults with MDD. The
letter said the application did not provide substantial evidence of the
effectiveness of Zurzuvae for treating of MDD and that additional
studies would be needed to support the approval.
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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/File Photo
Sage and Biogen said they were
reviewing the feedback and evaluating next steps.
Analysts have anticipated that the stocks of both companies would
fall if the drug was approved only for postpartum depression, due to
the smaller patient population.
Until now, the FDA said, treatment for postpartum depression was
available only as an intravenous injection.
In 2021, an estimated 21 million adults in the United States had at
least one episode of major depressive disorder, which is
characterized by a persistent feeling of sadness. PPD affects around
one in seven women who give birth.
(Reporting by Sriparna Roy, Lavanya Ahire and Gokul Pisharody in
Bengaluru; Editing by Krishna Chandra Eluri, Leslie Adler and
William Mallard)
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