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Therapeutic nihilism? Alzheimer's drug adoption in US slowed by scepticism – The Frontier Post

Therapeutic nihilism? Alzheimer's drug adoption in US slowed by scepticism – The Frontier Post
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Therapeutic nihilism? Alzheimer's drug adoption in US slowed by scepticism

Food and Drug Administration approved Leqembi last year

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Alzheimer's drug adoption in US slowed by doctors' skepticism

Alzheimer's drug adoption in US slowed by doctors' skepticism
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Alzheimer's drug adoption in US slowed by doctors' skepticism

CHICAGO (Reuters) -Nine months into the U.S. launch of the first drug proven to slow the advance of Alzheimer's, Eisai and Biogen's Leqembi is facing an unexpected hurdle to widespread use: an entrenched belief among some doctors that treating the memory-robbing disease is futile. Alzheimer's experts had anticipated bottlenecks due to Leqembi's requirements, which include additional diagnostic tests, twice-monthly infusions and regular brain scans to guard against potentially lethal side effects. And those issues have played a role in slow adoption since the drug was approved by the U.S. Food and Drug Administration, according to interviews with 20 neurologists and geriatricians from rural, urban, academic and community practices in 19 states.

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Alzheimer's Drug Adoption in US Slowed by Doctors' Skepticism

Alzheimer's Drug Adoption in US Slowed by Doctors' Skepticism
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Alzheimer's treatment: Drug adoption slow in U.S.

Nine months into the U.S. launch of the first drug proven to slow the advance of Alzheimer's, Eisai and Biogen's Leqembi is facing an unexpected hurdle to widespread use: an entrenched belief among some doctors that treating the memory-robbing disease is futile.

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Alzheimer's drug embrace slows down as US doctors' reluctance grows

The adoption of the FDA-approved Alzheimer's drug, Leqimbi, has slowed down in the U.S. as more experts grow hesitant about the drugs cost, risks and efficacy.

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Alzheimer's drug adoption in US slowed by doctors' skepticism | WSAU News/Talk 550 AM · 99.9 FM

(Repeats to additional subscribers with no changes to text ) By Julie Steenhuysen CHICAGO (Reuters) -Nine months into the U.S. launch of the first drug proven to slow the advance of Alzheimer's, Eisai and Biogen's Leqembi is facing an unexpected hurdle...

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Roche granted FDA Breakthrough Device Designation

Supporting earlier Alzheimer's disease diagnosis

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Roche granted FDA Breakthrough Device Designation for blood test to support earlier Alzheimer's disease diagnosis

The Elecsys® pTau217 plasma biomarker test is being developed as part of an ongoing partnership between Roche and Eli Lilly and CompanyOnce approved, the test will aid healthcare providers in...

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