
Japanese pharma major Eisai (TSE: 4523) and US biotech Biogen (Nasdaq: BIIB) said China's National Medical Products Administration (NMPA) has approved the subcutaneous autoinjector formulation of Leqembi (lecanemab) as an initiation treatment for mild cognitive impairment or mild dementia due to Alzheimer's disease, collectively termed early Alzheimer's disease.
The companies describe it as the first and only anti-amyloid therapy in China enabling at-home administration, and the second country globally, after the USA, to approve the subcutaneous initiation formulation.
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