Second approval in major market for Lilly’s Alzheimer’s drug
US drugmaker Eli Lilly's (NYSE: LLY) Kisunla (donanemab-azbt) has been approved in Japan for the treatment of patients with early symptomatic Alzheimer's disease (AD).
The 350mg/20 mL IV infusion will be administered every four weeks in these patients, who include people with mild cognitive impairment (MCI) as well as people with the mild dementia stage of AD, with confirmed amyloid pathology.
Japan is the second major market in which Kisunla has been approved for use, after the US approval in July 2024.
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