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0.000489740217576776 -0.000104551282403924 0 0.000500745615724558 0.00190943657864184 0.00186541498605071 0.00204150135641534 0.00204150135641534
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C2N Diagnostics Says FDA's Approval of Donanemab Highlights Its Role in Helping to Determine Alzheimer's Disease Pathology [Yahoo! Finance]

Eli Lilly and Company (LLY) 
Last eli lilly and company earnings: 4/23 06:25 am Check Earnings Report
US:NYSE Investor Relations: investor.lilly.com
Company Research Source: Yahoo! Finance
Food and Drug Administration to approve donanemab for treatment of early Alzheimer's disease. Researchers used C2N's Precivity-p-tau217 blood biomarker in its Phase 3 clinical trial and analysis for donanemab , which was highlighted in the article "Donanemab in Early Symptomatic Alzheimer Disease: The TRAILBLAZER-ALZ 2 Randomized Clinical Trial " in the Journal of the American Medical Association. Eli Lilly and Company says donanemab significantly slowed cognitive and functional decline in people with early symptomatic Alzheimer's disease. Exploratory outcomes included changes in plasma p-tau217 at 76 weeks and other time-based analyses. Lilly stresses that donanemab is not a cure for Alzheimer's disease, but it has been shown to slow disease progression in clinical trials. C2N believes it is uniquely positioned to support the medical community in confirming Alzheimer's disease pathology with its Precivity™ portfolio of tests. The PrecivityAD2™ blood test is a clinical care assay Show less Read more
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