By Jake Perez, Editor at LinkedIn News
A panel of advisers to the Food and Drug Administration has unanimously backed an experimental Alzheimer’s treatment, paving the way for an anticipated full FDA approval by July 6. The drug, lecanemab, which Eisai and Biogen will market as Leqembi, was shown to delay cognitive decline by 27% over 18 months, but there were some serious complications during clinical trials — including brain swelling, bleeding or microhemorrhages, and three deaths. Leqembi has been found to remove amyloid plaques from the brain, which can “contribute to the development of Alzheimer’s,” writes Axios.
- More than 6 million people live with Alzheimer’s in the U.S., according to the Alzheimer’s Association. That number is expected to more than double by 2050.
Eisai and Biogen’s Alzheimer’s drug gets FDA panel’s backing, setting the stage for broader use – The Boston Globe
bostonglobe.com • 4 min read
By Jacob Bell
Senior Reporter at Industry Drive
FDA panel backs full approval for Eisai, Biogen Alzheimer’s drug
biopharmadive.com • 4 min read
https://www.biopharmadive.com/news/fda-leqembi-advisers-vote-full-approval-alzheimers/652634/
✔ The FDA AdComm panel of outside advisers voted 6-0 that a large study confirmed the drug’s benefits for patients with mild or early Alzheimer’s. The nonbinding vote amounts to a recommendation for full approval, and the FDA is scheduled to issue a final decision on the matter by July 6.
#Alzheimers
#Biotechnology