Abstract

ObjectiveNI margins have to be chosen appropriately to control the risk of degradation of treatment effects in non-inferiority (NI) trials. We aimed to study whether the current choice of NI margins protects sufficiently against a degradation of treatment effect on an average.Study Design and SettingNI trials reflecting current practice were assembled and for each trial, the NI margin was translated into a likelihood of degradation. The likelihood of degradation was calculated as the conditional probability of a treatment being harmful given that it is declared non-inferior in the trial, using simulation. Its distribution among the NI trials was then studied to assess the potential risk of degradation.ResultsThe median (lower/upper quartile) NI margin among 112 binary outcome NI trials corresponded to an odds ratio of 0.57(0.45, 0.66), while among 38 NI trials with continuous outcome, to a Cohen’s d of −0.42(−0.54, −0.31) and a hazard ratio of 0.82(0.73, 0.86) among 24 survival outcome NI trials. Overall, the median likelihood of degradation was 56% (45%, 62%).ConclusionOnly two fifths of the current NI trials had a likelihood of degradation lower than 50%, suggesting that, in majority of the NI trials, there is no sufficient protection against degradation on an average. We suggest a third hurdle for the choice of NI margins, thus contributing a sufficient degree of protection.

Highlights

  • Non-inferiority (NI) trials have gained popularity over the years [1]

  • The median NI margin among 112 binary outcome NI trials corresponded to an odds ratio of 0.57(0.45, 0.66), while among 38 NI trials with continuous outcome, to a Cohen’s d of 20.42(20.54, 20.31) and a hazard ratio of 0.82(0.73, 0.86) among 24 survival outcome NI trials

  • Only two fifths of the current NI trials had a likelihood of degradation lower than 50%, suggesting that, in majority of the NI trials, there is no sufficient protection against degradation on an average

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Summary

Introduction

Though there are research areas where NI trials are not acceptable as a proof of efficacy for drug approval [2,3,4], NI trials are gaining importance in certain fields, as they are today a standard part of drug approval [5]. The aim of a NI trial is to show that a new treatment is not inferior to the standard treatment below a certain pre-specified margin called non-inferiority margin. Choice of this NI margin is a critical step in conducting NI trials. The narrower of the two margins should be used [8]

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