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    Group-Sequential Clinical Trials with Multiple Co-Objectives

    Group-Sequential Clinical Trials with Multiple Co-Objectives by Hamasaki, Toshimitsu; Asakura, Koko; Evans, Scott R.;

    Series: SpringerBriefs in Statistics; 0;

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      • Publisher's listprice EUR 69.54
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        29 498 Ft (28 094 Ft + 5% VAT)
      • Discount 20% (cc. 5 900 Ft off)
      • Discounted price 23 599 Ft (22 475 Ft + 5% VAT)

    29 498 Ft

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    Estimated delivery time: In stock at the publisher, but not at Prospero's office. Delivery time approx. 3-5 weeks.
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    Product details:

    • Edition number 1st ed. 2016
    • Publisher Springer
    • Date of Publication 10 June 2016
    • Number of Volumes 1 pieces, Book

    • ISBN 9784431558989
    • Binding Paperback
    • No. of pages113 pages
    • Size 235x155 mm
    • Weight 454 g
    • Language English
    • Illustrations 14 Illustrations, black & white
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    Long description:

    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.

    ?This book is a highly stimulating read for anyone who is interested in group-sequential trials, or anybody who wishes to learn about how studies with multiple endpoints can be made more efficient.? (Michael J. Grayling, Technometrics, Vol. 60 (3), 2018)?

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    Table of Contents:

    1. Introduction.- 2. Early Stopping for Efficacy in Clinical Trials with multiple co-primary endpoints.- 3. Sample size recalculation based on observed effects at interim.- 4. Early stopping for futility in Clinical Trials with multiple co-primary endpoints.- 5. Early stopping for futility or Efficacy in Clinical Trials with multiple co-primary endpoints.- 6. Clinical Trials with multiple primary endpoints.- 7. Group-sequential designs for three-arm noninferiority clinical trials.- 8. Further development: topics not covered in this book.

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    Group-Sequential Clinical Trials with Multiple Co-Objectives

    Group-Sequential Clinical Trials with Multiple Co-Objectives

    Hamasaki, Toshimitsu; Asakura, Koko; Evans, Scott R.;

    29 498 HUF

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