Novel trends in orphan market drug discovery: Amyotrophic lateral sclerosis as a case study

被引:1
作者
Clark, JE [1 ]
Brennan, A [1 ]
Ramesh, TM [1 ]
Heywood, JA [1 ]
机构
[1] ALS Therapy Dev Fdn, Newton, MA 02459 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2002年 / 7卷
关键词
amyotrophic lateral sclerosis; riluzole; drug development; orphan disease; orphan drug; SOD; superoxide dismutase; drug discovery; review;
D O I
10.2741/clark1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As new lead discovery technologies of high throughput screening and rational drug design have been incorporated into pharmaceutical and biotechnology drug discovery programs, researchers have focused on the applying these new technologies in diseases traditionally neglected by for-profit drug discovery efforts. This article reviews general trends in orphan disease lead discovery, identifies best practices of orphan market drug discovery and provides an overview of recent ALS lead discovery programs and drug development according to these metrics. Best practices in orphan market drug discovery embodied by programs like the NIH Anticonvulsant Screening Program include the (1) management of timelines and priorities, (2) engagement of for-profit partners, (3) creative application of technology, (4) collaboration, and (5) flexibility. Recent trends in ALS lead discovery have been shaped not only by the predominance of animal models of disease over in vitro models, but also by the successes and best practices of these earlier orphan market drug discovery programs. The ALS Treatment Initiative, the Johns Hopkins Center for ALS Research, the ALS Association, and the ALS Therapy Development Foundation have all initiated lead discovery programs in the past several years which seek to utilize existing experimental models of the disease and challenge assumptions about the linear nature of the lead discovery and development process. The compounds currently in clinical evaluation for ALS were identified as leads from a variety of sources, further reinforcing the transforming effect these new lead discovery programs have had on drug discovery and development in ALS. We conclude our review with an overview of the challenges and opportunities lead discovery in ALS currently faces, ultimately concluding that ALS lead discovery, and indeed orphan market drug discovery in general, would most benefit from more centralized lead discovery management, expanded national access to core facilities for lead discovery, and matrixed simultaneous screening of multiple compounds for multiple neglected diseases.
引用
收藏
页码:C83 / C96
页数:14
相关论文
共 167 条
  • [1] Season of birth in amyotrophic lateral sclerosis
    Ajdacic-Gross, V
    Wang, J
    Gutzwiller, F
    [J]. EUROPEAN JOURNAL OF EPIDEMIOLOGY, 1998, 14 (04) : 359 - 361
  • [2] ALEXIANU ME, 1994, J NEUROCHEM, V63, P2365
  • [3] Immune reactivity in a mouse model of familial ALS correlates with disease progression
    Alexianu, ME
    Kozovska, M
    Appel, SH
    [J]. NEUROLOGY, 2001, 57 (07) : 1282 - 1289
  • [4] Almer G, 2001, ANN NEUROL, V49, P176, DOI 10.1002/1531-8249(20010201)49:2<176::AID-ANA37>3.0.CO
  • [5] 2-X
  • [6] N-acetyl-L-cysteine improves survival and preserves motor performance in an animal model of familial amyotrophic lateral sclerosis
    Andreassen, OA
    Dedeoglu, A
    Klivenyi, P
    Beal, MF
    Bush, AI
    [J]. NEUROREPORT, 2000, 11 (11) : 2491 - 2493
  • [7] Increases in cortical glutamate concentrations in transgenic amyotrophic lateral sclerosis mice are attenuated by creatine supplementation
    Andreassen, OA
    Jenkins, BG
    Dedeoglu, A
    Ferrante, KL
    Bogdanov, MB
    Kaddurah-Daouk, R
    Beal, MF
    [J]. JOURNAL OF NEUROCHEMISTRY, 2001, 77 (02) : 383 - 390
  • [8] QUANTITATIVE MOTOR-ASSESSMENT IN AMYOTROPHIC-LATERAL-SCLEROSIS
    ANDRES, PL
    HEDLUND, W
    FINISON, L
    CONLON, T
    FELMUS, M
    MUNSAT, TL
    [J]. NEUROLOGY, 1986, 36 (07) : 937 - 941
  • [9] Immunosuppressant FK506 does not exert beneficial effects in symptomatic G93A superoxide dismutase-1 transgenic mice
    Anneser, JMH
    Gmerek, A
    Gerkrath, J
    Borasio, GD
    Heumann, R
    [J]. NEUROREPORT, 2001, 12 (12) : 2663 - 2665
  • [10] ANNUNZIATA P, 1985, ACTA NEUROL SCAND, V72, P61