Assessing the ratio of means as a causal estimand in clinical endpoint bioequivalence studies in the presence of intercurrent events
Author:
Affiliation:
1. Department of BiostatisticsUniversity of Iowa College of Public Health Iowa City Iowa
2. Office of Biostatistics, Center for Drug Evaluation and ResearchFood and Drug Administration (CDER/FDA) Silver Spring Maryland
Publisher
Wiley
Subject
Statistics and Probability,Epidemiology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/sim.8367
Reference40 articles.
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4. A taxonomy of estimands for regulatory clinical trials with discontinuations
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