ALZ-NET will collect real-world clinical practice data and outcomes to allow physicians to make more appropriate decisions in patient care as FDA approved therapies become available. Creation of a provider-enrolled patient registry for novel FDA-approved treatments for AD, and for the associated diagnostic tests and biomarkers, is meant to swiftly advance the science, as the pipeline is growing.

ALZ-NET will be a resource for evidence gathering, information sharing, and education across clinical and research communities, encouraging innovative, inclusive research and supporting opportunities to improve care. ALZ-NET aims to assess the clinical course of individuals from a variety of backgrounds and communities, to achieve representativeness beyond the populations historically enrolled in clinical trials.

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