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9781584889847

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! The first part of the book is a cohesive exploration of the uses of methods of multiple hypothesis testing. These chapters are understandable for a reader who wants to study multiple testing methods beyond the post-hoc tests presented in a course on design of experiments. ! The final chapter provides an accessible description of problems in testing data from microarrays. --Biometrics, September 2010 If you are a statistician in the pharmaceutical industry looking for a comprehensive description of multiple testing in a clinical trial, this book is for you. Each of the main sources of multiplicity in clinical trials, such as several doses, endpoints, interim analyses etc., are discussed in detail. On the way, you will encounter dose-finding, adaptive designs and even microarray experiments. The book can undoubtedly be of value to wider groups -- in fact we would rank it as the best book on multiplicity given its up-to-date material ! the book certainly attains its objective of being a modern summary of the approaches to multiplicity issues primarily in clinical trials, serving as an excellent guide for those who find themselves face to face with simultaneous testing and would like to have an overview over possible ways of tackling the problem. ! --Vera Lisovskaja and Carl-Fredrik Burman, Journal of Biopharmaceutical Statistics, Issue 6, 2010

If you are a statistician in the pharmaceutical industry looking for a comprehensive description of multiple testing in a clinical trial, this book is for you. Each of the main sources of multiplicity in clinical trials, such as several doses, endpoints, interim analyses etc., are discussed in detail. On the way, you will encounter dose-finding, adaptive designs and even microarray experiments. The book can undoubtedly be of value to wider groups -- in fact we would rank it as the best book on multiplicity given its up-to-date material ! the book certainly attains its objective of being a modern summary of the approaches to multiplicity issues primarily in clinical trials, serving as an excellent guide for those who find themselves face to face with simultaneous testing and would like to have an overview over possible ways of tackling the problem. ! --Vera Lisovskaja and Carl-Fredrik Burman, Journal of Biopharmaceutical Statistics, Issue 6, 2010

This book is an important contribution to the increasing literature about multiple testing. The book focuses on pharmaceutical statistics with emphasis on clinical research. The methodology and applications described are nonetheless relevant to other fields. ! The book's strength lies in the completeness in the topics covered and the updated nature of material presented. Most of the recently developed methods are results of investigations by the book's authors, who are the leading scientists in the field. ! I find this book well structured and having fairly well-interconnected chapters. This work has been conceived to suit perfectly the bookshelf of a clinical statistician in the pharmaceutical sector and is a valuable resource and reference for statisticians who are interested in the subject. --Gonzalo Duran Pacheco and F. Hoffmann-La Roche, Journal of the Royal Statistical Society: Series A, Vol. 174, October 2011 The book presents the subject matter in a way that is very thorough and is written by some of the top researchers in the field. ! the book is a good one and libraries should be encouraged to purchase a copy. It will be useful to those researchers in both the biomedical and statistics fields. Practising statisticians in industry stand to benefit most from the book because of its completeness. --Isaac Dialsingh, Journal of Applied Statistics, 2011 ! The first part of the book is a cohesive exploration of the uses of methods of multiple hypothesis testing. These chapters are understandable for a reader who wants to study multiple testing methods beyond the post-hoc tests presented in a course on design of experiments. ! The final chapter provides an accessible description of problems in testing data from microarrays. --Biometrics, September 2010 If you are a statistician in the pharmaceutical industry looking for a comprehensive description of multiple testing in a clinical trial, this book is for you. Each of the main sources of multiplicity in clinical trials, such as several doses, endpoints, interim analyses etc., are discussed in detail. On the way, you will encounter dose-finding, adaptive designs and even microarray experiments. The book can undoubtedly be of value to wider groups -- in fact we would rank it as the best book on multiplicity given its up-to-date material ! the book certainly attains its objective of being a modern summary of the approaches to multiplicity issues primarily in clinical trials, serving as an excellent guide for those who find themselves face to face with simultaneous testing and would like to have an overview over possible ways of tackling the problem. ! --Vera Lisovskaja and Carl-Fredrik Burman, Journal of Biopharmaceutical Statistics, Issue 6, 2010

Author Information

Alex Dmitrienko is a research advisor in Global Statistical Sciences at Eli Lilly and Company in Indianapolis, Indiana. Ajit C. Tamhane is senior associate dean and professor of industrial engineering and management sciences in the McCormick School of Engineering and Applied Science at Northwestern University in Illinois. Frank Bretz is a biometrical fellow of clinical information sciences at Novartis Pharma AG in Switzerland. He is also an adjunct professor at Hannover Medical School in Germany.

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