U.S. lawmakers to investigate approval, pricing of Alzheimer's drug from
Biogen
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[June 26, 2021]
(Reuters) -U.S. lawmakers on Friday announced an investigation into the
approval and pricing of Biogen Inc's Alzheimer's drug, Aduhelm, amid
concerns over its steep price and doubts if the clinical evidence proves
the drug works.
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The drug, which has a list price of $56,000 per year, was approved
by the U.S. regulators as the first treatment to attack a likely
cause of Alzheimer's on June 7.
"We have serious concerns about the steep price of Biogen's new
Alzheimer's drug Aduhelm and the process that led to its approval
despite questions about the drug's clinical benefit," House
Committee on Oversight and Reform said in a statement.
The investigation has been announced by Rep. Carolyn Maloney,
chairwoman of the Committee on Oversight and Reform, and Rep. Frank
Pallone, Jr., Chairman of the Committee on Energy and Commerce.
Biogen said it will "of course cooperate with any inquiry we may
receive from these committees," in response to a Reuters request for
comment.
At $56,000 a year, the Kaiser Family Foundation estimates that
Medicare could spend $57 billion or more per year on Aduhelm, which
is more than Medicare Part B spends on all other drugs combined, the
House Committee said.
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Health insurers and the
Medicare program will bear most of the cost of
the drug, whose price will vary based on dosage
and discounts.
The Food and Drug Administration (FDA) approved
the drug - despite strong objection from its own
expert advisory panel - for all patients with
Alzheimer's, although it has only been tested
for patients in the early stages of the disease.
Three of the 11 members of FDA's independent
advisory panel have resigned in protest over the
agency's decision.
Shares of the drugmaker were down nearly 1% in
after-market trading.
(Reporting by Dania Nadeem in Bengaluru;
additional reporting by Juby Babu; Editing by
Arun Koyyur)
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