Eligibility for New FDA-approved Alzheimer’s Drug

Published on July 7, 2023

The FDA has given its stamp of approval to Leqembi, a new drug developed by Eisai and Biogen, for patients with Alzheimer’s disease. This decision is like giving the green light to a brand new roller coaster ride that promises hope and relief for those affected by Alzheimer’s. With standard approval, Leqembi is set to be widely covered by the U.S. government’s Medicare health plan, making it more accessible to eligible patients. This is fantastic news because this drug has the potential to slow down the progression of the disease and improve quality of life for patients and their families. It’s like discovering a secret weapon against an enemy that has challenged us for far too long. With this milestone achieved, further research may focus on optimizing treatment plans and potentially developing even more effective drugs. To learn more about Leqembi and how it can make a difference in the lives of Alzheimer’s patients, dive into the fascinating research behind this breakthrough.

The U.S. Food and Drug Administration on Thursday granted standard approval to Eisai and Biogen’s Leqembi for patients with Alzheimer’s disease. The FDA decision is expected to trigger broader coverage of the $26,500-a-year drug by the U.S. government’s Medicare health plan…

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