Kieser M
Department of Biometry, Dr. Willmar Schwabe Pharmaceuticals, Karlsruhe, Germany.
Int J Clin Pharmacol Ther. 1995 Jul;33(7):388-90.
In the planning phase of a therapeutic equivalence trial, a range has to be specified that defines the parameter region within which the treatments to be compared are considered equal for practical purposes. It is current practice in equivalence assessment to fix some value for limiting the equivalence range and to test the corresponding null hypothesis in confirmatory analysis. This procedure is unsatisfactory, if, for example, the drug to be investigated is not only equivalent but turns out to be even superior to standard. In this situation it would be desirable to test not only for equivalence but also for superiority. The paper presents an alternative approach that allows for a flexible handling of the problem. If therapeutic equivalence can be established the method additionally allows, under maintenance of the multiple level, for testing all null hypotheses that correspond to acceptable equivalence ranges and even of superiority. Because of the special structure of the hypotheses no alpha-adjustment is needed for these additional confirmatory analyses.
在治疗等效性试验的规划阶段,必须指定一个范围,该范围定义了参数区域,在该区域内,出于实际目的,被比较的治疗方法被视为等效。在等效性评估中,当前的做法是固定某个值以限制等效范围,并在验证性分析中检验相应的零假设。如果例如待研究的药物不仅等效而且结果优于标准,那么这个程序是不令人满意的。在这种情况下,不仅希望检验等效性,还希望检验优越性。本文提出了一种替代方法,该方法允许灵活处理该问题。如果可以确立治疗等效性,该方法在保持多重性水平的情况下,还允许检验与可接受的等效范围相对应的所有零假设,甚至包括优越性假设。由于假设的特殊结构,这些额外的验证性分析不需要进行α调整。