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药物试验中单侧检验的应用:一位美国食品药品监督管理局咨询委员会成员的观点

The use of one-sided tests in drug trials: an FDA advisory committee member's perspective.

作者信息

Fisher L D

机构信息

Department of Biostatistics, Fred Hutchinson Cancer Research Center, University of Washington, Seattle 98155.

出版信息

J Biopharm Stat. 1991;1(1):151-6. doi: 10.1080/10543409108835012.

Abstract

The use of one-sided or two-sided tests in drug trials to evaluate new compounds is considered. For drugs that may be tested against placebos, with two positive trials required (as in the United States), it is argued that from both a regulatory and pharmaceutical industry perspective, one-sided tests at the 0.05 significance level are appropriate. In situations where only one trial against placebo may be done (for example, survival trials), one-sided tests at the 0.025 level are appropriate in many cases. For active control trials it is argued that two-sided tests are usually appropriate.

摘要

考虑在药物试验中使用单侧检验或双侧检验来评估新化合物。对于可能与安慰剂进行对比测试的药物(如在美国需要两项阳性试验),有人认为,从监管和制药行业的角度来看,在0.05显著性水平下进行单侧检验是合适的。在仅可能进行一项针对安慰剂的试验的情况下(例如生存试验),在许多情况下,在0.025水平下进行单侧检验是合适的。对于活性对照试验,有人认为通常进行双侧检验是合适的。

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