Operationalizing selection criteria for clinical trials in Alzheimer's disease: Biomarker and clinical considerations

Author:

Petersen Ronald C.1,Graf Ana2,Brady Chris3,De Santi Susan4,Florian Hana5,Landen Jaren6,Pontecorvo Mike7,Randolph Christopher3,Sink Kaycee M.8,Carrillo Maria C.9,Weber Christopher J.9

Affiliation:

1. Department of Neurology Mayo Clinic Rochester Minnesota USA

2. Novartis Pharma AG Basel Switzerland

3. WCG Clinical Endpoint Solutions, Princeton New Jersey USA

4. Neurology Business Group Eisai Nutley New Jersey USA

5. Abbvie North Chicago Illinois USA

6. Biogen Cambridge Massachusetts USA

7. Eli Lilly and Company Indianapolis Indiana USA

8. Genentech Inc. South San Francisco California USA

9. Alzheimer's Association Chicago Illinois USA

Abstract

AbstractAlzheimer's disease (AD) staging criteria lack standardized, empirical description. Well‐defined AD staging criteria are an important consideration in protocol design, influencing a more standardized inclusion/exclusion criteria and defining what constitutes meaningful differentiation among the stages. However, many trials are being designed on the basis of biomarker features and the two need to be coordinated. The Alzheimer's Association Research Roundtable (AARR) Spring 2021 meeting discussed the implementation of preclinical AD staging criteria, and provided recommendations for how they may best be incorporated into clinical trials research. Discussion also included what currently available tools for global clinical trials may best define populations in preclinical AD trials, and if are we able to differentiate preclinical from clinical stages of the disease. Well‐defined AD staging criteria are key to improving early detection, diagnostics, clinical trial enrollment, and identifying statistically significant clinical changes, and researchers discussed how emerging blood biomarkers may help with more efficient screening in preclinical stages.

Publisher

Wiley

Subject

Psychiatry and Mental health,Neurology (clinical)

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