Abstract
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 secondstep 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.
| Original language | English |
|---|---|
| Pages (from-to) | 331-336 |
| Number of pages | 6 |
| Journal | Drug Information Journal |
| Volume | 45 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - May 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
User-Defined Keywords
- Clinical trial
- Conditional test
- Noninferiority
- Superiority
- Type I error rate
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