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Groupsequential Clinical Trials With Multiple Coobjectives 1st Edition Toshimitsu Hamasaki

  • SKU: BELL-5485798
Groupsequential Clinical Trials With Multiple Coobjectives 1st Edition Toshimitsu Hamasaki
$ 31.00 $ 45.00 (-31%)

5.0

110 reviews

Groupsequential Clinical Trials With Multiple Coobjectives 1st Edition Toshimitsu Hamasaki instant download after payment.

Publisher: Springer Japan
File Extension: PDF
File size: 2.07 MB
Pages: 118
Author: Toshimitsu Hamasaki, Koko Asakura, Scott R. Evans, Toshimitsu Ochiai (auth.)
ISBN: 9784431558989, 9784431559009, 4431558985, 4431559000
Language: English
Year: 2016
Edition: 1

Product desciption

Groupsequential Clinical Trials With Multiple Coobjectives 1st Edition Toshimitsu Hamasaki by Toshimitsu Hamasaki, Koko Asakura, Scott R. Evans, Toshimitsu Ochiai (auth.) 9784431558989, 9784431559009, 4431558985, 4431559000 instant download after payment.

This book focuses on group sequential methods for clinical trials with co-primary endpoints based on the decision-making frameworks for: (1) rejecting the null hypothesis (stopping for efficacy), (2) rejecting the alternative hypothesis (stopping for futility), and (3) rejecting the null or alternative hypothesis (stopping for either futility or efficacy), where the trial is designed to evaluate whether the intervention is superior to the control on all endpoints. For assessing futility, there are two fundamental approaches, i.e., the decision to stop for futility based on the conditional probability of rejecting the null hypothesis, and the other based on stopping boundaries using group sequential methods. In this book, the latter approach is discussed. The book also briefly deals with the group sequential methods for clinical trials designed to evaluate whether the intervention is superior to the control on at least one endpoint. In addition, the book describes sample size recalculation and the resulting effect on power and type I error rate. The book also describes group sequential strategies for three-arm clinical trials to demonstrate the non-inferiority of experimental intervention to actively control and to assess the assay sensitivity to placebo control.

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