| Literature DB >> 26710325 |
Serge Gauthier1, Marilyn Albert2, Nick Fox3, Michel Goedert4, Miia Kivipelto5, Jorge Mestre-Ferrandiz6, Lefkos T Middleton7.
Abstract
The success rate of the pharmaceutical research and development (R&D) for dementia drugs has been abysmally low, in the last two decades. Also low has been the number of pipeline drugs in development, compared to other therapy areas. However, the rationale of early terminations has not been reported in the majority of trials. These are key findings of the recently published pharmaceutical pipeline analysis by the UK-based Office of Health Economics (OHE). Our understanding of main challenges include (1) the significant gaps of knowledge in the nosology and complexity of the underpinning biological mechanisms of the commonest, not familial, forms of late onset dementias; (2) low signal-to-noise ratio, notwithstanding the lack of validated biomarkers as entry and/or end-point criteria; (3) recruitment and retention, particularly in the asymptomatic and early disease stages. A number of current and future strategies aimed at ameliorating drug development are outlined and discussed.Entities:
Keywords: Alzheimer's; Amyloid hypothesis; Attrition; Clinical trials; Dementia; Research & development
Mesh:
Substances:
Year: 2015 PMID: 26710325 DOI: 10.1016/j.jalz.2015.12.003
Source DB: PubMed Journal: Alzheimers Dement ISSN: 1552-5260 Impact factor: 21.566