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Cognition endpoints for Parkinson's disease: A roadmap for developing patient-focused assessment tools to accelerate drug development.

Cognition endpoints for Parkinson's disease: A roadmap for developing patient-focused assessment tools to accelerate drug development.

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Where did the research take place?

The study site has not been established. Author addresses may differ from where the research occurred.

Reading, GB · Author affiliation

PCOA Associates Ltd, Reading, UK.
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US · Author affiliation · country only

Cogstate Ltd, New Haven, CT, USA.
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Tucson, US · Author affiliation

Critical Path Institute, Tucson, AZ, USA.
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New York City, US · Author affiliation

The Michael J. Fox Foundation for Parkinson's Research, New York, NY, USA.
Location evidence

Chicago, US · Author affiliation

Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
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Philadelphia, US · Author affiliation

Department of Psychiatry, University of Pennsylvania, Philadelphia, PA, USA.
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Bulle, CH · Author affiliation

UCB, Bulle, Switzerland.
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Original abstract

Cognitive dysfunction is a prevalent and impactful feature of Parkinson's disease (PD), with substantial heterogeneity in onset, severity, and progression, and a high lifetime risk of dementia. Despite its clinical importance, effective treatments and fit-for-purpose outcome measures remain limited. This article reports outcomes from a multi-stakeholder roundtable convened by The Michael J. Fox Foundation for Parkinson's Research, outlining priorities to advance patient-focused endpoints and improve clinical trial design to accelerate therapeutic development for cognitive dysfunction. In the context of the current understanding of cognitive impairment across the PD/dementia with Lewy bodies (DLB) spectrum and existing neuropsychological assessment approaches, recommendations are made regarding necessary literature reviews, including qualitative data and related conceptual models, disease models including pathophysiology and neuropsychological profile, and clinical outcome assessment (COA) reviews, including content validity, psychometrics, and fitness-for-purpose. Additionally, novel conceptual models of cognitive impairment across the normal, mild cognitive impairment (MCI) and dementia spectrum are needed and may require further qualitative evidence.

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