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Two-Stage Adaptive Designs for Three-Treatment Bioequivalence Studies
Bioequivalence (BE) studies are most often conducted as crossover trials, and therefore establishing their required sample size necessitates specification of the within-person variance. Given that this specification is often difficult in practice, there has been great interest in recent years in the...
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| 出版年: | Stat Biopharm Res |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7612189/ https://ncbi.nlm.nih.gov/pubmed/35003526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/19466315.2019.1654911 |
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