The failure of the antidepressant drug discovery process is systemic

被引:41
|
作者
Hendrie, Colin
Pickles, Alasdair
机构
[1] Institute of Psychological Sciences, University of Leeds, Woodhouse Lane
[2] Institute of Membranes and Systems Biology, University of Leeds, Leeds
[3] Department of Neuroscience, Physiology and Pharmacology, University College London, Gower Street
基金
英国医学研究理事会;
关键词
Animal models; antidepressant; depression; drug discovery; MDD; ANIMAL-MODELS; VALIDITY;
D O I
10.1177/0269881112466185
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Current antidepressants are crude compared with the ideal and patents on most have expired. There are therefore strong clinical and commercial pressures for new drugs to replace them. The prospects for this are, however, now markedly reduced as several major pharmaceutical companies have abandoned work in this area whilst many others have sharply decreased their research investment. These changes and the lack of progress over such a long period are indicative of a catastrophic systems failure which, it is argued, has been caused in large part by a logical flaw at the animal modelling stage. This tautology has served to lock the current antidepressant drug discovery process into an iterative loop capable only of producing further variations of that which has gone before. Drugs produced by this approach have proved to be only poorly effective in the context of the clinically depressed population as a whole. Hence, the inevitable failure of the current antidepressant drug discovery process has left little behind that can be salvaged. Therefore, it is suggested that this be urgently reformulated on more rational grounds using more appropriate species in new animal models based upon a thorough understanding of the behavioural expressions of depression in the clinic.
引用
收藏
页码:407 / 416
页数:10
相关论文
共 50 条
  • [41] Improving early part of drug discovery process
    Anon
    1600, Society of Chemical Industry
  • [42] Needed: system dynamics for the drug discovery process
    Sirois, Suzanne
    Cloutier, L. Martin
    DRUG DISCOVERY TODAY, 2008, 13 (15-16) : 708 - 715
  • [43] RECEPTOR-BINDING IN THE DRUG DISCOVERY PROCESS
    WILLIAMS, M
    MEDICINAL RESEARCH REVIEWS, 1991, 11 (02) : 147 - 184
  • [44] FLEDGLING FIRM TARGETS DRUG DISCOVERY PROCESS
    BAUM, R
    CHEMICAL & ENGINEERING NEWS, 1990, 68 (10) : 10 - 11
  • [45] Will genetics really revolutionize the drug discovery process?
    Gelbert, LM
    Gregg, RE
    CURRENT OPINION IN BIOTECHNOLOGY, 1997, 8 (06) : 669 - 674
  • [46] The hit-to-lead process in drug discovery
    Gillespie, P
    Goodnow, RA
    ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 39, 2004, 39 : 293 - 304
  • [47] The application of conformal prediction to the drug discovery process
    Martin Eklund
    Ulf Norinder
    Scott Boyer
    Lars Carlsson
    Annals of Mathematics and Artificial Intelligence, 2015, 74 : 117 - 132
  • [48] Will genetics really revolutionize the drug discovery process?
    Gelbert, L. M.
    Gregg, R. E.
    Current Opinion in Biotechnology, 8 (06):
  • [49] The application of conformal prediction to the drug discovery process
    Eklund, Martin
    Norinder, Ulf
    Boyer, Scott
    Carlsson, Lars
    ANNALS OF MATHEMATICS AND ARTIFICIAL INTELLIGENCE, 2015, 74 (1-2) : 117 - 132
  • [50] The drug discovery and development process in the new millennium
    Levy, MD
    CANADIAN JOURNAL OF GASTROENTEROLOGY, 2000, 14 (07): : 641 - 643