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Adaptive Design Theory and Implementation Using SAS and R

List Price: $89.99
SKU:
9781138034235
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  • Product Details

    Author:
    Mark Chang
    Format:
    Paperback
    Pages:
    706
    Publisher:
    CRC Press (October 14, 2016)
    Language:
    English
    ISBN-13:
    9781138034235
    Weight:
    46.625oz
    Dimensions:
    6.125" x 9.1875"
    File:
    TAYLORFRANCIS-TayFran_260110060643920-20260110.xml
    Folder:
    TAYLORFRANCIS
    List Price:
    $89.99
    Series:
    Chapman & Hall/CRC Biostatistics Series
    Case Pack:
    55
    As low as:
    $85.49
    Publisher Identifier:
    P-CRC
    Discount Code:
    H
    Audience:
    Professional and scholarly
    Country of Origin:
    United States
    Pub Discount:
    30
    Imprint:
    Chapman and Hall/CRC
  • Overview

    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.