Suitability of the Clinical Dementia Rating‐Sum of Boxes as a single primary endpoint for Alzheimer's disease trials-Reference-Cited by-同舟云学术

Suitability of the Clinical Dementia Rating‐Sum of Boxes as a single primary endpoint for Alzheimer's disease trials

Published:2011-07-11 Issue:6 Volume:7 Page:602
ISSN:1552-5260
Container-title:Alzheimer's & Dementia
language:en
Short-container-title:Alzheimer's & Dementia

Author:

Coley Nicola¹,Andrieu Sandrine¹²,Jaros Mark³,Weiner Michael⁴,Cedarbaum Jesse³,Vellas Bruno¹⁵

Affiliation:

1. INSERM U558—University of Toulouse IIIF‐31073ToulouseFrance

2. Department of Epidemiology and Public Health CHU ToulouseToulouseFrance

3. Elan PharmaceuticalsSouth San FranciscoCAUSA

4. Department of Veterans Affairs Medical CenterUniversity of CaliforniaSan FranciscoCAUSA

5. Department of Geriatric Medicine Alzheimer Centre, CHU ToulouseGerontopoleToulouseFrance

Funder

French Ministry of Health

CIFRE

Ipsen Pharma and the French National Association of Technical Research

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Clinical Neurology,Developmental Neuroscience,Health Policy,Epidemiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1016/j.jalz.2011.01.005

Reference33 articles.

1. EMEA Committee for Medicinal Products for Human Use (CHMP).Guideline on medicinal products for the treatment of Alzheimer's disease and other dementias. In: European Medicines Agency (EMEA) Pre‐Authorisation Evaluation of Medicines for Human Use; July 24 2008; London UK. Doc. Ref. CPMP/EWP/553/95 Rev. 1

2. Alzheimer's Biomarker Initiative Hits Its Stride

3. Endpoints for trials in Alzheimer's disease: a European task force consensus

4. A new rating scale for Alzheimer's disease

5. A Neuropsychological Test Battery for Use in Alzheimer Disease Clinical Trials

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