FDA reviews new Alzheimer's drug LEQEMBI, which could offer home-based treatment via autoinjector.

The FDA has accepted the Biologics License Application for LEQEMBI, a drug for early Alzheimer's disease, for subcutaneous maintenance dosing. If approved, LEQEMBI will be the only FDA-approved treatment for Alzheimer's that can be self-administered at home using an autoinjector, potentially simplifying treatment and reducing the need for hospital visits. The drug aims to clear amyloid plaques in the brain and, if approved, could be used by patients with mild cognitive impairment or early-stage dementia. The FDA's decision is expected by August 31, 2025.

2 months ago
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