Runner
with Alzheimer's hopes new drug will keep him on track
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[June 09, 2021]
By Julie Steenhuysen
CHICAGO (Reuters) -For Bill McKay, 69, of
Haslett, Michigan, the U.S. approval of Biogen Inc's controversial
Alzheimer's drug on Monday offers hope that the veteran of 29 marathons
can keep on running.
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For his wife, Jill McKay, 66, an office manager, it offers the hope
that he will not get lost along the way.
"He can be running in a familiar location and still get disoriented
and that's a big worry for me. I work full time," she said.
The drug, called Aduhelm, is the first treatment ever approved to
target a cause of Alzheimer's, with the aim of slowing progression
of the mind-robbing disease.
The U.S. Food and Drug Administration approved the treatment despite
contradictory evidence in two large clinical trials, in which the
drug showed a benefit in one but not in the other, and after a panel
of outside experts said the data failed to prove that the medicine
works.
More than 900 centers are ready to start intravenous infusions in as
soon as two weeks, at a cost of about $56,000 per year.
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Bill McKay, a former coordinator in a lab that has been working on
COVID-19 vaccines, was diagnosed with Alzheimer's last year and has
what he describes as "entry level" disease, including memory
problems and trouble navigating. He can no longer drive a car, but
he is able to care for himself.
He is among several patients seen by neurologist Dr. Cara Leahy of
Memorial Healthcare in Owosso, Michigan, who has been prequalified
as appropriate for treatment with Biogen's drug. The hospital
arranged for Reuters to speak with the couple and Dr. Leahy.
The FDA has required a confirmatory trial to demonstrate that the
Biogen treatment works as intended to slow cognitive and functional
decline by removing amyloid plaques from the brain, but that could
take years.
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 Although the FDA approved the
drug broadly for treatment of Alzheimer's
dementia, Leahy said she plans to offer it to
patients in the earliest stages of the disease -
the group tested in clinical trials.
She sees a big challenge to educate patients
about the risks of the drug and the limited
evidence of its efficacy. Biogen has estimated
that around 1.5 million Americans are eligible
for Aduhelm.
Patients must understand, "this is not a cure,"
Leahy said. "We are hoping that it has some
ability to slow down the progression for
patients."
It is not clear yet how much the drug will cost
patients, most of whom are expected to be
covered by the U.S. government's Medicare
program for people aged 65 and older.
Patients will likely have some out-of-pocket
costs such as for coinsurance and a deductible,
but so far Medicare has not made a decision. The
McKays are waiting for guidance from their
insurance company and Medicare.
They still need to learn more about what the
drug can and cannot do, as well as side effects
and other limitations.
"We have an appointment with Dr Leahy next
week," Jill McKay said.
(Reporting by Julie Steenhuysen; Editing by
Peter Henderson and Bill Berkrot)
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