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Trial participants treated with Kisunla had up to a 39% lower risk of progressing to the next clinical stage of disease than those taking placebo.
July 3, 2024
By: Kristin Brooks
Managing Editor, Contract Pharma
Eli Lilly and Co. received approval from the FDA for Kisunla (donanemab-azbt, 350 mg/20 mL once-monthly injection for IV infusion) an Alzheimer’s treatment for adults with early symptomatic Alzheimer’s disease (AD), which includes people with mild cognitive impairment (MCI) as well as people with the mild dementia stage of AD, with confirmed amyloid pathology. Once-monthly Kisunla is the first and only amyloid plaque-targeting therapy with evidence to support stopping therapy whe...
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