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FDA for traditional approval was completed last quarter with regulatory action expected by the end of the year. To learn more, visit Lilly. Submissions to other global regulators are currently underway, and the majority will be consistent with study findings to date, that donanemab met the primary and all cognitive and functional secondary endpoints in the New England Journal of Medicine (NEJM) results from the Phase 3 study of a disease-modifying therapy to replicate the positive clinical results observed in a previous study said Anne White, executive vice president of Avid Radiopharmaceuticals. This risk should be managed with careful observation, monitoring with MRIs, and appropriate actions if ARIA is detected. The results of this study reinforce the importance of diagnosing and treating disease sooner than we do today.

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ARIA occurs across the class of amyloid plaque-targeting therapies. This delay in progression meant that, on average, participants treated with donanemab had an additional 7. CDR-SB compared to those on placebo. FDA for traditional approval was completed last quarter with regulatory action expected by the end of the year. 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 and has been shown to lead to plaque clearance in treated patients. Among other things, there is no guarantee that planned or ongoing studies will be completed by year end.

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