FDA grants approval for at-home Leqembi start
Eisai (TYO: 4523) and Biogen (Nasdaq: BIIB) have secured US approval for patients to begin treatment with an at-home version of their Alzheimer’s medicine Leqembi Iqlik (lecanemab-irmb), removing the need to start therapy through intravenous infusions.
The US Food and Drug Administration (FDA) approved a supplemental Biologics License Application covering once-weekly subcutaneous initiation dosing in adults with early Alzheimer’s disease. This includes patients with mild cognitive impairment or mild dementia caused by the condition.
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