Improving clinical trials - American Society of Clinical Psychopharmacology recommendations

被引:27
作者
Klein, DF
Thase, ME
Endicott, J
Adler, L
Glick, I
Kalali, A
Leventer, S
Mattes, J
Ross, P
Bystritsky, A
机构
[1] New York State Psychiat Inst & Hosp, New York, NY 10032 USA
[2] Columbia Univ, New York, NY 10032 USA
[3] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[4] Western Psychiat Inst & Clin, Pittsburgh, PA USA
[5] Clin Insights, Glen Burnie, MD USA
[6] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[7] Quintiles Inc, San Diego, CA USA
[8] Univ Calif Irvine, Irvine, CA USA
[9] Vela Pharmaceut, Lawrenceville, NJ USA
[10] Psychopharmacol Res Princeton, Princeton, NJ USA
[11] Amer Soc Clin Psychopharmacol Inc, New York, NY USA
[12] Natl Fdn Depress Illness, New York, NY USA
[13] Univ Calif Los Angeles, Los Angeles, CA USA
关键词
D O I
10.1001/archpsyc.59.3.272
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The major purpose of this American Society of Clinical Psychopharmacology-sponsored meeting was to identify strategies for more efficiently detecting clinical drug effects, thus reducing the economic and scientific risks of investigating new chemical entities in psychiatric disorders. The meeting consisted of presentations and discussions by experts who repeatedly had difficulty pursuing scientific, public health-relevant goals. Many approaches to improving the detection of potentially beneficial agents were reviewed. In this article, we discuss technically feasible study improvements. The scope of inquiry included identifying means of shifting institutional and regulatory assumptions and processes, even to the point of seeking appropriate national incentives.
引用
收藏
页码:272 / 278
页数:7
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