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Alzheimer’s Drug Maker Expects FDA Approval This Summer

FDA approval would expand Medicare coverage for the $26,500/year drug, but rollout could take years.

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According to a recent CNBC article, Japanese drugmaker Eisai expects the FDA to fully approve its Alzheimer's treatment Leqembi this summer. Leqembi, which was developed with Biogen, is an expensive new antibody that has shown promise in slowing the progression of Alzheimer's disease in people over the age of 65.  The company estimates that 100,000 people are expected to receive an early Alzheimer's diagnosis and become eligible for Leqembi by 2026, though the number of undiagnosed people is almost certainly higher.

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