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frrol

09/16/25 12:45 PM

#500742 RE: Doc328 #500725

Yes, minimum MMSE or similar would very likely be a prescription exclusion. (Wonder if this could be disregarded for private payers in Europe.)
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09/16/25 2:12 PM

#500766 RE: Doc328 #500725

I’d like to see a large RCT to definitively answer function, subgroup efficacy (ADCLEAR1 vs ADCLEAR3), and biomarkers (brain atrophy, p42/40). In oncology and even with donanemab, regulators have often allowed approval first with a confirmatory trial. Given blarcamesine’s safety profile and cognitive benefit, I’m wondering what criteria CHMP uses to decide between granting approval with a confirmatory trial versus requiring a new trial upfront — curious how you see it?