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A two-way enriched clinical trial design: combining advantages of placebo lead-in and randomized withdrawal

机译:双向丰富的临床试验设计:结合安慰剂导入和随机退出的优势

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摘要

A new clinical trial design, designated the two-way enriched design (TED), is introduced, which augments the standard randomized placebo-controlled trial with second-stage enrichment designs in placebo non-responders and drug responders. The trial is run in two stages. In the first stage, patients are randomized between drug and placebo. In the second stage, placebo non-responders are re-randomized between drug and placebo and drug responders are re-randomized between drug and placebo. All first-stage data, and second-stage data from first-stage placebo non-responders and first-stage drug responders, are utilized in the efficacy analysis. The authors developed one, two and three degrees of freedom score tests for treatment effect in the TED and give formulae for asymptotic power and for sample size computations. The authors compute the optimal allocation ratio between drug and placebo in the first stage for the TED and compare the operating characteristics of the design to the standard parallel clinical trial, placebo lead-in and randomized withdrawal designs. Two motivating examples from different disease areas are presented to illustrate the possible design considerations.
机译:引入了一种新的称为双向富集设计(TED)的临床试验设计,该试验通过在安慰剂无反应者和药物应答者中进行的第二阶段富集设计来增强标准的随机安慰剂对照试验。试用分为两个阶段。在第一阶段,患者在药物和安慰剂之间随机分组。在第二阶段中,安慰剂无反应者在药物和安慰剂之间重新分配,而毒品反应者在药物和安慰剂之间重新分配。所有第一阶段数据以及来自第一阶段安慰剂无反应者和第一阶段药物反应者的第二阶段数据都用于功效分析。作者针对TED中的治疗效果开发了一个,两个和三个自由度得分测试,并给出了渐近能力和样本量计算的公式。作者计算了TED的第一阶段药物和安慰剂之间的最佳分配比例,并将设计的操作特征与标准平行临床试验,安慰剂导入和随机退出设计进行了比较。给出了来自不同疾病领域的两个激励示例,以说明可能的设计考虑因素。

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