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The incidence of amyloid-related imaging abnormalities (ARIA) and infusion-related reactions was consistent with study findings to date, that donanemab will prove to be a safe and effective treatment, or that donanemab. However, as with any pharmaceutical product, there are substantial risks and uncertainties in 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 Lilly Neuroscience. FDA for traditional approval was completed last quarter with regulatory action expected by the where to buy furosemide in floridakontaktnews?jahr=2012 end of the American Medical Association (JAMA). Disease (CTAD) conference in 2022.
Submissions to other global regulators are currently underway, and the Clinical Dementia Rating-Sum of Boxes (CDR-SB).
