Biomarkers in psychotropic drug development

被引:5
作者
Ahmed, S [1 ]
Mozley, PD [1 ]
Potter, WZ [1 ]
机构
[1] Lilly Res Labs, Indianapolis, IN USA
关键词
D O I
10.1176/appi.ajgp.10.6.678
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The authors review the use of biomarkers in the development of novel psychotropic agents. They briefly review clinical drug development, emphasizing the importance of incorporating biomarkers. For the development of psychotropic agents, biomarkers are particularly useful for assessing central nervous system exposure and effects and for serving as surrogate measures for safety and efficacy. Collectively, biomarkers allow for more accurate estimation of doses for clinical trials as drug development progresses, For drugs that target the pathophysiology of Alzheimer disease, several promising biomarkers are becoming available that may allow improved signal detection in clinical trials. Procedures for developing new drugs are evolving rapidly. Technical advances in the field are making it possible to shift from empirically-based methods to mechanistically-driven schemes, Biomarkers enhance the quality and safety of clinical drug development and reduce its cost and duration.
引用
收藏
页码:678 / 686
页数:9
相关论文
共 113 条
[11]   Diagnostic approaches to Alzheimer's disease [J].
Boss, MA .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2000, 1502 (01) :188-200
[12]  
Cherry Simon R., 1996, P191
[13]  
CHIPKIN RE, 1988, J PHARMACOL EXP THER, V247, P1093
[14]   Measurement of human brain dexfenfluramine concentration by 19F magnetic resonance spectroscopy [J].
Christensen, JD ;
Yurgelun-Todd, DA ;
Babb, SM ;
Gruber, SA ;
Cohen, BM ;
Renshaw, PF .
BRAIN RESEARCH, 1999, 834 (1-2) :1-5
[15]  
Christian BT, 1996, J PHARMACOL EXP THER, V279, P325
[16]  
Colburn WA, 2000, J CLIN PHARMACOL, V40, P1419
[17]  
Cutler NR, 1998, REV NEUROL-FRANCE, V154, pS131
[18]  
Cutler NR, 1998, ACTA NEUROL SCAND, V97, P244
[19]   Symptom provocation studies in psychiatric disorders: Scientific value, risks, and future [J].
D'Souza, DC ;
Berman, RM ;
Krystal, JH ;
Charney, DS .
BIOLOGICAL PSYCHIATRY, 1999, 46 (08) :1060-1080
[20]   Activated Alzheimer disease platelets retain more beta amyloid precursor protein [J].
Davies, TA ;
Long, HJ ;
Sgro, K ;
Rathbun, WH ;
McMenamin, ME ;
Seetoo, K ;
Tibbles, H ;
Billingslea, AM ;
Fine, RE ;
Fishman, JB ;
Levesque, CA ;
Smith, SJ ;
Wells, JM ;
Simons, ER .
NEUROBIOLOGY OF AGING, 1997, 18 (02) :147-153