DESIGN AND ANALYSIS ISSUES FOR CROSSOVER DESIGNS IN PHASE I CLINICAL STUDIES
Author:
Affiliation:
1. a Faculty of Applied Mathematics , University of Twente , P.O. Box 217, Enschede, 7500 AE, The Netherlands
2. b Centre for Biometry Wageningen, CPRO-DLO , P.O. Box 16, Wageningen, 6700 AA, The Netherlands
Publisher
Informa UK Limited
Subject
Pharmacology (medical),Pharmacology,Statistics and Probability
Link
https://www.tandfonline.com/doi/pdf/10.1081/BIP-100101003
Reference10 articles.
1. Design and Analysis of Cross-Over Trials
2. Statistical methods for a three-period crossover design in which high dose cannot be used first
3. Is the ‘simple carry-over’ model useful?
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