Design and Analysis of Cross-Over Trials
3rd Edition
Published on 8. October 2014
Book
Hardback
438 pages
978-1-4398-6142-4 (ISBN)
Description
Design and Analysis of Cross-Over Trials is concerned with a specific kind of comparative trial known as the cross-over trial, in which subjects receive different sequences of treatments. Such trials are widely used in clinical and medical research, and in other diverse areas such as veterinary science, psychology, sports science, and agriculture.
The first edition of this book was the first to be wholly devoted to the subject. The second edition was revised to mirror growth and development in areas where the design remained in widespread use and new areas where it had grown in importance. This new Third Edition:
Contains seven new chapters written in the form of short case studies that address re-estimating sample size when testing for average bioequivalence, fitting a nonlinear dose response function, estimating a dose to take forward from phase two to phase three, establishing proof of concept, and recalculating the sample size using conditional power
Employs the R package Crossover, specially created to accompany the book and provide a graphical user interface for locating designs in a large catalog and for searching for new designs
Includes updates regarding the use of period baselines and the analysis of data from very small trials
Reflects the availability of new procedures in SAS, particularly proc glimmix
Presents the SAS procedure proc mcmc as an alternative to WinBUGS for Bayesian analysis
Complete with real data and downloadable SAS code, Design and Analysis of Cross-Over Trials, Third Edition provides a practical understanding of the latest methods along with the necessary tools for implementation.
The first edition of this book was the first to be wholly devoted to the subject. The second edition was revised to mirror growth and development in areas where the design remained in widespread use and new areas where it had grown in importance. This new Third Edition:
Contains seven new chapters written in the form of short case studies that address re-estimating sample size when testing for average bioequivalence, fitting a nonlinear dose response function, estimating a dose to take forward from phase two to phase three, establishing proof of concept, and recalculating the sample size using conditional power
Employs the R package Crossover, specially created to accompany the book and provide a graphical user interface for locating designs in a large catalog and for searching for new designs
Includes updates regarding the use of period baselines and the analysis of data from very small trials
Reflects the availability of new procedures in SAS, particularly proc glimmix
Presents the SAS procedure proc mcmc as an alternative to WinBUGS for Bayesian analysis
Complete with real data and downloadable SAS code, Design and Analysis of Cross-Over Trials, Third Edition provides a practical understanding of the latest methods along with the necessary tools for implementation.
Reviews / Votes
"Jones and Kenward added several valuable case studies to the third edition of their book. The case studies illustrate elegantly the applications of recent innovations in statistical methodologies to cross-over trials. The new edition is an excellent reference for scientists who want to understand cross-over trials or are interested in learning how statistical advancements in the last decade could be used to expand the versatility of cross-over trials."-Christy Chuang-Stein, Ph.D., Vice President, Head of Statistical Research and Consulting Center, Pfizer Inc.
"As in the previous two editions, this edition offers a comprehensive coverage on the design and analysis of cross-over trials. With several major noteworthy updates, it will assist statisticians to conveniently tackle practical issues that arise in a cross-over trial... The most substantial update is the addition of seven new chapters (Chapters 8-14) in the form of short case studies. These real-world examples cover a wide range of issues and solutions above and beyond what is commonly encountered in a cross-over trial and significantly broaden the book...the third edition of Design and Analysis of Cross-Over Trials remains an outstanding reference for statisticians who work on cross-over trials, whether occasionally or frequently."
-Haiying Chen, Wake Forest School of Medicine, in Journal of the American Statistical Association, Volume 111, 2016
"Jones and Kenward present students, academics, and researchers with the third edition of their text, dedicated to an understanding of a comparative trait known as the cross-over trial, through which patients involved in a study received different sequences of treatments. New for the third edition, the text includes seven new chapters devoted to case studies, coverage of the R package Crossover, updates related to the use of period baselines and the analysis of very small trials, and a variety of other features."
-Ringgold, Inc. Book News, February 2015
Praise for the Second Edition:
"In the second edition, updated from the original published in 1989, the authors have added discussions of new, more comprehensive (downloadable) datasets and some additional topics. ... Substantially updated with more than 130 new references, the book has been thoroughly modernized to reflect new developments in this area. Among the new material added to the book is a chapter on bioequivalence and a discussion of new methods for longitudinal and categorical data. This book continues to be a recommended choice as a valuable reference for clinical statisticians and those who study medical trials where treatments through cross-over design are a feasible approach. For those who already own the first edition, updating to the second will help keep you current on recent developments in this area."
-Journal of the American Statistics Association
More details
Series
Edition
3rd edition
Language
English
Place of publication
Boca Raton
United States
Publishing group
Taylor & Francis Inc
Target group
College/higher education
Professional and scholarly
Academic
Illustrations
51 s/w Abbildungen, 200 s/w Tabellen
200 Tables, black and white; 51 Illustrations, black and white
Dimensions
Height: 240 mm
Width: 161 mm
Thickness: 28 mm
Weight
822 gr
ISBN-13
978-1-4398-6142-4 (9781439861424)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Byron Jones | Michael G. Kenward
Design and Analysis of Cross-Over Trials
Book
10/2024
3rd Edition
Chapman & Hall/CRC
€79.41
Shipment within 10-20 days
Byron Jones | Michael G. Kenward
Design and Analysis of Cross-Over Trials
E-Book
10/2014
3rd Edition
Chapman & Hall/CRC
€63.49
Available for download
Byron Jones | Michael G. Kenward
Design and Analysis of Cross-Over Trials
E-Book
10/2014
3rd Edition
Chapman and Hall
€63.49
Available for download
Previous edition
Book
03/2003
1st Edition
Chapman and Hall
€60.99
Article exhausted; check for reprint
Persons
Byron Jones is a senior biometrical fellow and executive director in the Statistical Methodology Group at Novartis Pharmaceuticals. Previously he was a senior statistical consultant/senior director at Pfizer and a senior director and UK head of the Research Statistics Unit at GlaxoSmithKline. In addition to 14 years of experience in the pharmaceutical industry, he has 25 years of experience in academia, ultimately holding the position of professor of medical statistics at De Montfort University. Currently he is an honorary professor at the London School of Hygiene and Tropical Medicine, visiting professor at University College London and at the University of Leicester, and a visiting professorial fellow at Queen Mary, University of London.
Michael G. Kenward is GlaxoSmithKline professor of biostatistics at the London School of Hygiene and Tropical Medicine. Previously he held positions at the Universities of Kent and Reading in the UK, and at research institutes in the UK, Iceland, and Finland. He has acted as a pharmaceutical industry consultant in biostatistics for more than 25 years. His research interests include the analysis of longitudinal data and cross-over trials, and modeling in biostatistics, with a particular interest in the problem of missing data. He has co-authored three textbooks and is well known for his 1994 Royal Statistical Society read paper on missing data.
Michael G. Kenward is GlaxoSmithKline professor of biostatistics at the London School of Hygiene and Tropical Medicine. Previously he held positions at the Universities of Kent and Reading in the UK, and at research institutes in the UK, Iceland, and Finland. He has acted as a pharmaceutical industry consultant in biostatistics for more than 25 years. His research interests include the analysis of longitudinal data and cross-over trials, and modeling in biostatistics, with a particular interest in the problem of missing data. He has co-authored three textbooks and is well known for his 1994 Royal Statistical Society read paper on missing data.
Content
Introduction. The 2x2 Cross-Over Trial. Higher-Order Designs for Two Treatments. Designing Cross-Over Trials. Analysis of Continuous Data. Analysis of Discrete Data. Bioequivalence Trials. Case Study: Phase I Dose-Response Noninferiority Trial. Case Study: Choosing a Dose-Response Model. Case Study: Conditional Power. Case Study: Proof of Concept Trial with Sample Size Re-Estimation. Case Study: Blinded Sample Size Re-Estimation in a Bioequivalence Study. Case Study: Unblinded Sample Size Re-Estimation in a Bioequivalence Study That Has a Group Sequential Design. Case Study: Various Methods for an Unblinded Sample Size Re-Estimation in a Bioequivalence Study. Appendix A: Least Squares Estimation. Bibliography.