Abstract:A three-arm non-inferiority trial including a placebo is usually utilized to assess the non-inferiority of an experimental treatment to a reference treatment. Existing methods for assessing non-inferiority mainly focus on the fully observed endpoints. However, in some clinical trials, treatment endpoints may be subject to missingness for various reasons, such as the refusal of subjects or their migration. To address this issue, this paper aims to develop a non-parametric approach to assess the non-inferiority … Show more
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