On assessment of bioequivalence under a higher-order crossover design
Author:
Affiliation:
1. a Biostatistics Department , Bristol-Myers Squibb Company , Plainsboro, New Jersey, 08536
2. b Biostatistics Department , Berlex Laboratories, Inc. , Wayne, New Jersey, 07470
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
https://www.tandfonline.com/doi/pdf/10.1080/10543409208835042
Reference18 articles.
1. A comparison of the Two One-Sided Tests Procedure and the Power Approach for assessing the equivalence of average bioavailability
2. The Two-Period Change-Over Design and Its Use in Clinical Trials
3. Symmetrical Confidence Intervals for Bioequivalence Trials
4. An Alternative Approach for the Assessment of Bioequivalence Between Two Formulations of a Drug
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