Por: NBC 6 South Florida World January 06, 2023
Getty Images MRI image of brain showing area of Alzheimer patient. data-ellipsis=false> The Food and Drug Administration on Friday granted accelerated approval for the Alzheimer's drug lecanemab, the second treatment from and its Japanese partner Eisai to receive an early green light in less than two years. The FDA's approval comes after clinical trial results published in November indicated that lecanemab slows cognitive decline... + full article
CNBC USA Health January 06, 2023
In this articleMRI image of brain showing area of Alzheimer patient.Getty ImagesThe Food and Drug Administration on Friday granted accelerated approval for the Alzheimer's drug lecanemab, the second treatment from and its Japanese partner Eisai to receive an early green... + más
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Los Angeles Times USA Science December 30, 2022
The Food and Drug Administration’s contentious approval of a questionable Alzheimer’s drug took another hit Thursday as congressional investigators called the process “rife with irregularities.” The 18-month investigation by two House committees detailed “atypical... + más
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ABC7 USA Health December 01, 2022
treatment, according to new Phase 3 trial results, but the findings raise some safety concerns because of its association with certain serious adverse events.Lecanemab has become one of the first experimental dementia drugs to appear to slow the progression of cognitive... + más
Alzheimer's drug trial shown to slow cognitive decline in long fight against dementia | CNBC
CNBC USA Health November 30, 2022
Alzheimer's is the most common form of dementia, a general term for loss of memory, language, and other thinking abilitiesBrian B. Bettencourt Toronto Star Getty ImagesA trial of an experimental Alzheimer's drug has been hailed as a new era in the beleaguered fight to... + más
Experimental drug appears to slow progression of Alzheimer's disease but raises safety concerns | ABC7
The Advocate USA Health November 16, 2022
What is the Lumipulse test for Alzheimer’s disease?In May, the U.S. Food and Drug Administration permitted marketing of the Lumipulse (G B-Amyloid Ratio [1-42/1-40]) test to Fujirebio Diagnostics, Inc. of Malvern, Pennsylvania. The test, which was granted Breakthrough Device... + más
Why Isn’t There an Effective Alzheimer’s Treatment Yet? | Slate
Forbes USA Tech October 22, 2022
A person walks on a suspended rope bridge in the clouds. Extreme attraction.getty This article is the fourth installment in my series on Alzheimer’s disease. Read more about Alzheimer’s disease in , , and of the series. The pharmaceutical and biotech companies, Eisai and... + más
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The Advocate USA Health September 17, 2022
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