Adaptive Design Theory And Implementation Using Sas And R Second Edition

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Adaptive Design Theory and Implementation Using SAS and R, Second Edition

Adaptive Design Theory and Implementation Using SAS and R, Second Edition
Author :
Publisher : CRC Press
Total Pages : 709
Release :
ISBN-10 : 9781482256598
ISBN-13 : 1482256592
Rating : 4/5 (592 Downloads)

Book Synopsis Adaptive Design Theory and Implementation Using SAS and R, Second Edition by : Mark Chang

Download or read book Adaptive Design Theory and Implementation Using SAS and R, Second Edition written by Mark Chang and published by CRC Press. This book was released on 2014-12-01 with total page 709 pages. Available in PDF, EPUB and Kindle. Book excerpt: Get Up to Speed on Many Types of Adaptive Designs Since the publication of the first edition, there have been remarkable advances in the methodology and application of adaptive trials. Incorporating many of these new developments, Adaptive Design Theory and Implementation Using SAS and R, Second Edition offers a detailed framework to understand the use of various adaptive design methods in clinical trials. New to the Second Edition Twelve new chapters covering blinded and semi-blinded sample size reestimation design, pick-the-winners design, biomarker-informed adaptive design, Bayesian designs, adaptive multiregional trial design, SAS and R for group sequential design, and much more More analytical methods for K-stage adaptive designs, multiple-endpoint adaptive design, survival modeling, and adaptive treatment switching New material on sequential parallel designs with rerandomization and the skeleton approach in adaptive dose-escalation trials Twenty new SAS macros and R functions Enhanced end-of-chapter problems that give readers hands-on practice addressing issues encountered in designing real-life adaptive trials Covering even more adaptive designs, this book provides biostatisticians, clinical scientists, and regulatory reviewers with up-to-date details on this innovative area in pharmaceutical research and development. Practitioners will be able to improve the efficiency of their trial design, thereby reducing the time and cost of drug development.


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