Takeda's treatment becomes first oral therapy for esophageal condition
in US
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[February 13, 2024]
(Reuters) -Takeda Pharmaceutical's therapy for an allergic
inflammation of the esophagus has received approval from the U.S. FDA,
the Japanese drugmaker said on Monday, capping a years-long regulatory
process.
The U.S. health regulator's approval makes the therapy the first oral
treatment for the condition, which currently only has Sanofi and
Regeneron's injection Dupixent.
The therapy, to be sold as Eohilia, will be used to treat eosinophilic
esophagitis (EoE) for 12 weeks in children above 11 years and adults.
In the chronic condition, a type of white blood cell called eosinophil
builds up in the esophagus lining, which can inflame or injure the
tissue, making it difficult for the individual to eat food.
Takeda's treatment will be available in stick packs of 2 milligram doses
by the end of February, the company said. The company has set wholesale
acquisition cost for the therapy, given twice daily, at $1,875 per
month.
The list price of Dupixent, given every week or every other week, for
all EoE patients is $3,803.20 per carton containing 2 pre-filled pens.
Takeda's treatment was initially in the run to be the first
U.S.-approved treatment for EoE, but was beaten to it by Dupixent.
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Takeda Pharmaceutical Co's logo is seen at its new headquarters in
Tokyo, Japan, July 2, 2018. REUTERS/Kim Kyung-Hoon/ File photo
The FDA had initially declined to
approve Takeda's treatment in 2021, and asked the drugmaker for an
additional clinical study in order to help resolve the regulator's
feedback.
After the rejection, the company discontinued clinical development
of the therapy, which it got through its $62 billion acquisition of
Shire, and took an impairment for the financial year ended March 31,
2022.
But the Japanese firm reanalyzed the older data and, after a
discussion with the FDA, resubmitted its application in September
for approval as a shorter 12-week treatment.
Takeda said it will reverse its impairment loss on Eohilia in the
fiscal year ending March 2024, but does not anticipate the impact to
be material.
(Reporting by Sriparna Roy in Bengaluru; Editing by Krishna Chandra
Eluri and Sriraj Kalluvila)
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