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Design and Analysis Considerations in Clinical Trials With a Sensitive

时间:2012-06-05

Title(题目):Design and Analysis Considerations in Clinical Trials With a Sensitive

Subpopulation

Speaker(报告人):Prof.Yan Daniel Zhao,University of Oklahoma Health Sciences Center at Tulsa

Time(时间):2012年6月7日(周四)下午03:15-04:15

Place(地点):成人直播-成人直播室 新楼217教室

Abstract(摘要):We present research on clinical trials with a sensitive subpopulation of patients, that is, a subgroup that is more likely to benefit from the treatment than the overall population. Given a sensitive subgroup defined by a prespecified classifier, for example, a clinical marker or pharmacogenomic marker, the trial’s outcome is declared positive if the treatment effect is established in the overall population or in the subgroup. We provide a summary of key considerations in clinical trials with a sensitive subgroup, including multiplicity and enrichment adjustments as well as optimality considerations in the analysis strategy. The methodology proposed in this article is illustrated using a neuroscience clinical trial and its operating characteristics are accessed via a simulation study.

Key Words: Clinical trials; Enriched clinical trials; Sensitive population; Type I error rate control; Weighted power.

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