Great Britain first European country to authorize Alzheimer’s drug Leqembi
Leqembi (lecanemab) has been granted a marketing authorization by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA, Japanese drugmaker Eisai (TYO: 4523) and US biotech Biogen (Nasdaq: BIIB) announced today.
Lecanemab is indicated for the treatment of mild cognitive impairment (MCI) and mild dementia due to Alzheimer’s disease (AD) in adult patients that are apolipoprotein E ε4 (ApoE ε4) heterozygotes or non-carriers.
As a result, Lecanemab becomes the first treatment for early AD (MCI and mild dementia due to AD) that targets an underlying cause of the disease, to be authorized in a country in Europe.
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