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發(fā)表于 2025-3-21 18:44:24 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Group-Sequential Clinical Trials with Multiple Co-Objectives
編輯Toshimitsu Hamasaki,Koko Asakura,Toshimitsu Ochiai
視頻videohttp://file.papertrans.cn/389/388968/388968.mp4
叢書名稱SpringerBriefs in Statistics
圖書封面Titlebook: ;
出版日期Book 2016
版次1
doihttps://doi.org/10.1007/978-4-431-55900-9
isbn_softcover978-4-431-55898-9
isbn_ebook978-4-431-55900-9Series ISSN 2191-544X Series E-ISSN 2191-5458
issn_series 2191-544X
The information of publication is updating

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發(fā)表于 2025-3-21 21:40:10 | 只看該作者
板凳
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發(fā)表于 2025-3-22 08:13:34 | 只看該作者
Interim Evaluation of Efficacy in Clinical Trials with Two Primary Endpoints,wo interventions based on two primary endpoints. In this situation, there are many procedures for controlling the Type I error rate. We discuss the simplest procedure, i.e., the weighted Bonferroni procedure which is commonly applied in practice. We evaluate the behavior of the sample size, power, a
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發(fā)表于 2025-3-22 09:43:39 | 只看該作者
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發(fā)表于 2025-3-22 12:53:59 | 只看該作者
Future Developments,her design features. This includes clinical trials with more than two interventions (e.g., dose-selection clinical trials): trials with time-to-event endpoints and trials with targeted subgroups and enrichment clinical trial designs. In Chap. ., we briefly discuss the issues in the design of these t
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發(fā)表于 2025-3-23 02:32:12 | 只看該作者
Philanthropy and Settler Colonialismuss several decision-making frameworks for evaluating efficacy or futility based on boundaries using group-sequential methodology. We incorporate the correlations among the endpoints into the calculations for futility critical boundaries and evaluate the required sample sizes as a function of design
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發(fā)表于 2025-3-23 07:10:36 | 只看該作者
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