On January
6th, the Food and Drug Administration approved, via the Accelerated Approval pathway, a new
treatment for Alzheimer’s disease called Leqembi. While older Alzheimer’s drugs
may ease symptoms for a time, they do nothing to stop the relentless downward
course of the disease. Leqembi is the second of a new class of drugs that are
designed to slow the progression of the disease.
“This treatment option is the latest therapy to target and
affect the underlying disease process of Alzheimer’s, instead of only treating
the symptoms of the disease,” said Dr. Billy Dunn, director of the Office of Neuroscience
in the FDA’s Center for Drug Evaluation and Research. Here are five things to
know about the new Alzheimer’s drug, Leqembi.
How effective is
Leqembi?
The new treatment may slow declines in memory and thinking
skills in those in the early stages of Alzheimer’s disease, but it is not a
cure. The drug is what’s known as a monoclonal antibody, designed to target the
beta-amyloid plaques that build up in the brains of those with Alzheimer’s
disease. It is made by the drug companies Esai and Biogen, and was tested under
the name lecanamab. (In 2021, the FDA approved another monoclonal antibody for
Alzheimer’s called Aduhelm, but in tests it seems that it was not as effective
as Leqembi; its efficacy remains controversial and it has some potentially deleterious
side effects. As a consequence it is not widely prescribed.)
In studies in nearly 1,800 patients over 18 months, Leqembi
slowed disease progression by 27 percent compared to a placebo – equivalent to
about a five-month delay in the disease getting worse. But both groups still
showed declines in cognitive skills, and any benefits were modest. On an
18-point scale of memory and thinking skills, those getting the treatment
scored about a half-point higher, which experts caution may not be noticeable
to patients in their everyday lives. It’s unknown whether the treatment may
have benefits over longer periods; continued testing is underway.
Who might benefit
from Leqembi?
The treatment showed modest benefits in those in the early
stages of Alzheimer’s disease and in those with mild cognitive impairment,
which often progresses to full-blown Alzheimer’s. But it probably won’t help
those with more advanced disease, when damage to the brain has become
extensive. Nor would it be expected to help those who have dementia that is not
caused by the amyloid plaques of Alzheimer’s. Indeed, patients that are
candidates for the treatment must first get a brain scan to confirm that there
is evidence of beta-amyloid buildup in the brain.
How is the
treatment administered?
Leqembi is given as an intravenous injection every two weeks,
typically at a clinic or hospital. Patients getting the infusions may
experience flu-like chills, fever and other side effects.
Is Leqembi
safe?
The treatment with Leqembi, and with antibodies in general,
carries risks. In tests, about 13 percent of people receiving the medication
showed evidence of brain swelling, compared to less than 2 percent taking a
placebo. About 17 percent had small bleeds in the brain, compared to about 9 percent
of those in the placebo group. Several people who were receiving the drug have
died of brain hemorrhages, including two who were also taking blood thinning
medications, though the drug makers say the deaths were not a result of
Leqembi. Still, experts caution that special caution is warranted, especially
in anyone taking blood thinners, which doctors commonly prescribe to prevent or
treat strokes. Patients may need to be monitored with brain scans to assess
brain bleeding and swelling, which may cause symptoms such as headaches or
dizziness.
How much does
Leqembi cost?
The drug is expected to become available in the coming months at
an average cost of $26,500 a year. That’s on top of any additional costs for
administering the medication and follow-up testing. It is unknown at this time
whether Medicare or other health insurance plans will cover some or all of the
costs.
By ALZinfo.org, The Alzheimer’s Information
Site. Reviewed by Marc Flajolet, Ph.D., Fisher Center for Alzheimer’s Research
Foundation at The Rockefeller University.
Source: Food and Drug Administration, Esai, Biogen
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