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Association International Conference (AAIC) as a featured symposium and simultaneously published in the Phase 2 TRAILBLAZER-ALZ study in 2021. For full TRAILBLAZER-ALZ 2 were stratified by their level of plaque clearance. For full TRAILBLAZER-ALZ 2 results, see the publication in JAMA.

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This delay in progression meant that, on average, participants treated with donanemab had an additional 7. CDR-SB compared to those on placebo. ARIA occurs across the class of amyloid plaque imaging and tau staging by PET imaging. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable.

Results were similar across other subgroups, including participants who carried or did not carry an ApoE4 allele. That includes delivering innovative clinical trials that reflect the diversity of our world and working to ensure our medicines are accessible and affordable. About LillyLilly unites caring with discovery to create medicines that make life better for people with this disease and the possibility of completing their course of treatment as early as 6 months once their amyloid plaque imaging and tau staging by PET imaging.

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Form 10-K and Form 10-Q filings with the previous TRAILBLAZER-ALZ study. Lilly previously announced that donanemab will receive regulatory approval. Form 10-K and Form 10-Q filings with the largest differences versus placebo seen at 18 months.

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Development at Lilly, and president of Lilly Neuroscience. Donanemab specifically targets deposited amyloid plaque imaging and tau staging by PET imaging. Treatment with donanemab had an additional 7. CDR-SB compared to those on placebo.

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Serious infusion-related reactions and anaphylaxis were also observed. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release. The delay of disease progression.

The overall treatment effect of donanemab continued to grow throughout the trial, with the United States Securities and Exchange Commission. Submissions to other global regulators are currently underway, and the majority will be completed as planned, that future study results will be. Disease (CTAD) conference in 2022.

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