Conditional Type I Error Rate for Superiority Test Conditioned on Establishment of Noninferiority in Clinical Trials

被引:2
作者
Yuan, Jiacheng [1 ]
Tong, Tiejun [2 ]
Ng, Tie-Hua [3 ]
机构
[1] Astellas Pharma Global Dev Inc, Res Data Sci, Deerfield, IL USA
[2] Univ Colorado, Dept Appl Math, Boulder, CO 80309 USA
[3] US FDA, Ctr Biol Evaluat & Res, Rockville, MD 20857 USA
来源
DRUG INFORMATION JOURNAL | 2011年 / 45卷 / 03期
关键词
Clinical trial; Conditional test; Noninferiority; Superiority; Type I error rate;
D O I
10.1177/009286151104500312
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
In clinical trials, it is often desirable to test for superiority conditioned on establishment of noninferiority based on the same primary endpoint. According to a guidance document issued by the European regulatory agency Committee for Proprietary Medicinal Products in 2001, no type I error rate adjustment is necessary for switching between superiority and noninferiority because the family-wise type I error rate is controlled at the same nominal level. However, Ng raised the issues of switching between superiority and noninferiority even though there is no inflation of the family-wise type I error rate and showed that the false discovery rate could be increased. To alleviate these concerns, we propose to control the conditional type I error rate of the second-step superiority test at the nominal significance level, which leads to a lower (unconditional) significance level of the second-step superiority test. The suggested adjustment posts a more rigorous condition to claim superiority, which is an effort to decrease the number of erroneous claims of superiority.
引用
收藏
页码:331 / 336
页数:6
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