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This was despite some concerns outlined in briefing documents regarding Lilly’s trial methodology, including its use of the integrated Alzheimer’s Disease Rating Scale (iADRS) as the primary endpoint, the use of tau protein levels to decide study inclusion and the cessation of donanemab treatment in patients whose brain amyloid levels dropped past a certain, pre-specified threshold
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Meanwhile Medex is using a marketing page claiming compliance with USP benchmarks
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