Gain-function optimisation of graphical multiple testing procedures for confirmatory clinical trials
确证性临床试验中图形多重检验程序的收益函数优化AI 解读 ↓
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确证性临床试验中图形多重检验程序的收益函数优化AI 解读 ↓
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Graphical multiple testing procedures are a flexible and transparent way to control the family-wise error rate when a confirmatory trial pursues several label claims, but they leave open the question of which graph to use. In practice sponsors often fall back on fixed-sequence or Holm procedures that may poorly reflect what the trial is actually trying to achieve. We propose to instead choose the graph that maximises an explicit gain function, which states what each possible set of rejected hypotheses is worth to the sponsor: typically nothing until a regulatory hurdle is cleared, then an incremental amount for each further claim. Conventional power criteria are recovered as special cases, and because the search is confined to graphical procedures, family-wise error rate control holds whichever graph is selected. We set out a structured procedure for eliciting the gain function from the clinical, commercial, and regulatory members of a trial team. The proposed framework also handles uncertainty in the treatment effects and correlations assumed at the design stage, by averaging performance over their plausible values rather than fixing a single assumption. For group sequential designs, we describe how it can further reward early claims. Five examples, drawn from real and hypothetical pharmaceutical trials, show that the best graph depends on how trial success is defined, how uncertain the design assumptions are, and, in a group sequential setting, when claims can be established.
We study inference for continuous linear functionals of solutions to ill-posed inverse problems, including Euclidean parameters arising in nonparametric instrumental variables, proximal causal inference, and shadow-variable models. Although pointwise root-$n$ inference is possible under standard conditions, we show that this need not translate into locally reliable inference. Under a model imposing only minimal regularity conditions, the target is Hellinger discontinuous…
We study nonparametric inference for a continuous-treatment causal dose-response curve and its first derivative under unmeasured confounding, using treatment- and outcome-inducing proxies. We establish a proximal doubly robust pseudo-outcome whose conditional mean given treatment equals the dose-response curve whenever either bridge function is correctly specified. Their (smoothed) efficient influence function representations lead to cross-fitted local-polynomial estimators…
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Generative AI has dramatically accelerated the rate at which new treatments---from novel pharmaceuticals to online marketing campaigns---can be conceived and deployed. As a result, modern experimentation platforms often run continuously, with treatments added as they are ready and removed when they underperform. We formalize this "Always-On" experimental setting, in which treatments can be dynamically generated, added to, and removed from a running experiment, and study the…