Sample Size Determination for a Three-Arm Equivalence Trial of Normally Distributed Responses
Author:
Affiliation:
1. Department of Statistics, Temple University, Philadelphia, Pennsylvania, USA
2. Office of Biostatistics, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
https://www.tandfonline.com/doi/pdf/10.1080/10543406.2014.948552
Reference9 articles.
1. Design and Analysis of Bioavailability and Bioequivalence Studies
2. Sample size determination for proving equivalence based on the ratio of two means for normally distributed data
3. Statistical assessment of biosimilarity based on relative distance between follow-on biologics
4. Assessing non-inferiority of a new treatment in a three-arm clinical trial including a placebo
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