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ALZ-507 is an orally administered small molecule drug being developed by Alzheon for the treatment of Alzheimer's disease. It is designed as a next-generation follow-on to Alzheon's lead candidate, valiltramiprosate (ALZ-801). ALZ-507 targets upstream amyloid aggregation to inhibit the formation of neurotoxic soluble amyloid oligomers, which are considered key drivers of Alzheimer's pathology. Additionally, the drug incorporates an APOE4 corrector mechanism of action, potentially enhancing its anti-oligomer effects. Developed for once-daily oral administration, ALZ-507 aims to provide improved gastrointestinal tolerability and a favorable safety profile. It is currently in Phase 1 clinical development.
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