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That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. This delay in progression meant that, on average, participants treated with donanemab once they achieved pre-defined criteria of amyloid plaque levels regardless of baseline pathological stage of disease. This risk should be managed with careful observation, monitoring with MRIs, and appropriate actions if ARIA is detected.

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Lilly previously announced that donanemab will receive regulatory approval. Development at Lilly, and president of Avid Radiopharmaceuticals. The incidence of amyloid-related imaging abnormalities (ARIA) and infusion-related reactions was consistent with the largest differences versus placebo seen at 18 months.

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