4.1 Review

Advances in the therapy of Alzheimer's disease: targeting amyloid beta and tau and perspectives for the future

Journal

EXPERT REVIEW OF NEUROTHERAPEUTICS
Volume 15, Issue 1, Pages 83-105

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1586/14737175.2015.995637

Keywords

Alzheimer's disease; amyloid beta immunotherapy; bapineuzumab; biological markers; clinical trials; prevention; randomized controlled trials center dot systems biology; solanezumab; tau immunotherapy

Funding

  1. AXA Research Fund
  2. Fondation Universite Pierre et Marie Curie
  3. 'Fondation pour la Recherche sur Alzheimer', Paris, France
  4. program 'Investissements d'avenir' [ANR-10-IAIHU-06]
  5. Boehringer-Ingelheim
  6. Bristol-Myers Squibb
  7. Elan Corporation
  8. Novartis
  9. Eisai Inc.
  10. Pfizer Inc.
  11. Sanofi-Aventis
  12. Roche Pharmaceuticals and Diagnostics
  13. GE Healthcare
  14. Avid
  15. Eli Lilly and Company
  16. GlaxoSmithKline-Biologicals
  17. Jung-Diagnostics
  18. Cytox
  19. Takeda
  20. Isis Pharmaceutical Inc.
  21. NIH [P50 AG05142, NIA U01-AG10483, NIA U01-AG024904, NIA R01-AG030048, R01-AG16381]
  22. California Department of Health Services
  23. Academy of Finland
  24. Swedish Research Council
  25. Alzheimer Association
  26. EU
  27. Fonds de la recherche en sante du Quebec (FRSQ)
  28. Eli Lilly

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Worldwide multidisciplinary translational research has led to a growing knowledge of the genetics and molecular pathogenesis of Alzheimer's disease (AD) indicating that pathophysiological brain alterations occur decades before clinical signs and symptoms of cognitive decline can be diagnosed. Consequently, therapeutic concepts and targets have been increasingly focused on early-stage illness before the onset of dementia; and distinct classes of compounds are now being tested in clinical trials. At present, there is a growing consensus that therapeutic progress in AD delaying disease progression would significantly decrease the expanding global burden. The evolving hypothesis- and evidence-based generation of new diagnostic research criteria for early-stage AD has positively impacted the development of clinical trial designs and the characterization of earlier and more specific target populations for trials in prodromal as well as in pre- and asymptomatic at-risk stages of AD.

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