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Half blind superiority tests for clinical trials of anti‐infective drugs
Author(s) -
Follmann Dean,
Brittain Erica,
Lumbard Keith
Publication year - 2018
Publication title -
statistics in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.996
H-Index - 183
eISSN - 1097-0258
pISSN - 0277-6715
DOI - 10.1002/sim.7954
Subject(s) - confidence interval , covariate , medicine , pointwise , statistics , drug , clinical trial , univariate , point estimation , mathematics , pharmacology , multivariate statistics , mathematical analysis
This paper introduces a test of superiority of new anti‐infective drug B over comparator drug A based on a randomized clinical trial. This test can be used to demonstrate assay (trial) sensitivity for noninferiority trials and rigorously tailor drug choice for individual patients. Our approach uses specialized baseline covariates X A , X B , which should predict the benefits of drug A and drug B, respectively. Using a response surface model for the treatment effect, we test for superiority at the ( X A , X B ) point that is most likely to show superiority. We identify this point based on estimates from a novel half‐blind pseudo likelihood, where we augment a blinded likelihood (mixed over the treatment indicator) with likelihoods for the overall success rates for drug A and drug B (mixed over X A , X B ). The augmentation results in much better estimates than those based on the mixed blinded likelihood alone but, interestingly, the estimates almost behave as if they were based on fully blinded data. We also develop an analogous univariate method using X A for settings where X B has little variation. Permutation methods are used for testing. If the “half‐blind” test rejects, pointwise confidence interval can be used to identify patients who would benefit from drug B. We compare the new tests to other methods with an example and via simulations.