US FDA withdraws approval for Covis Pharma's preterm birth prevention
drug
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[April 07, 2023]
(Reuters) -The U.S. Food and Drug Administration (FDA) on
Thursday withdrew its approval for Covis Pharma's preterm birth
prevention drug, Makena, saying that the drug was not effective in
treating the complication.
The U.S. health regulator has been pushing to withdraw the drug since
2020 but Covis insisted that the FDA wait for data from another
confirmatory study and narrow its use in the meantime.
The withdrawal of the clearance for Makena provided under the
accelerated approval pathway, will also apply to cheaper copycat
versions of the drug, the FDA said in a statement.
In March, Covis had voluntarily withdrawn its application for full
approval of the drug and said it would outline its plan for winding-down
supplies from the market after the regulator made a final decision.
The company did not immediately respond to a Reuters request for comment
on their plans to withdraw the drug.
The FDA advised patients to talk to their healthcare provider while
recognizing that there is a supply of Makena and its generics that have
already been distributed.
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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
Makena and its generic versions are
the only approved treatments for reducing the risk of preterm birth,
which affects one in every 10 babies in the United States.
The drug was granted accelerated approval in 2011 but ensuing
studies did not verify the clinical benefit of the drug. Private
equity-backed Covis gained the drug through a $647 million deal for
Amag Pharmaceuticals, the seller of Makena, in 2020.
In October, a panel of external advisers to the FDA had almost
unanimously recommended withdrawal of the drug from the market after
a failed study.
Makena, a hormonal medicine, was approved based on data that showed
it reduced the rate of preterm deliveries, rather than evidence that
it improved the health of babies.
(Reporting by Khushi Mandowara and Leroy Leo in Bengaluru; Editing
by Rashmi Aich)
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