Literature DB >> 18932136

A comparison of methods for adaptive treatment selection.

Tim Friede1, Nigel Stallard.   

Abstract

Traditionally drug development is generally divided into three phases which have different aims and objectives. Recently so-called adaptive seamless designs that allow combination of the objectives of different development phases into a single trial have gained much interest. Adaptive trials combining treatment selection typical for Phase II and confirmation of efficacy as in Phase III are referred to as adaptive seamless Phase II/III designs and are considered in this paper. We compared four methods for adaptive treatment selection, namely the classical Dunnett test, an adaptive version of the Dunnett test based on the conditional error approach, the combination test approach, and an approach within the classical group-sequential framework. The latter two approaches have only recently been published. In a simulation study we found that no one method dominates the others in terms of power apart from the adaptive Dunnett test that dominates the classical Dunnett by construction. Furthermore, scenarios under which one approach outperforms others are described.

Mesh:

Year:  2008        PMID: 18932136     DOI: 10.1002/bimj.200710453

Source DB:  PubMed          Journal:  Biom J        ISSN: 0323-3847            Impact factor:   2.207


  9 in total

1.  Twenty-five years of confirmatory adaptive designs: opportunities and pitfalls.

Authors:  Peter Bauer; Frank Bretz; Vladimir Dragalin; Franz König; Gernot Wassmer
Journal:  Stat Med       Date:  2015-03-16       Impact factor: 2.373

2.  Maximum type 1 error rate inflation in multiarmed clinical trials with adaptive interim sample size modifications.

Authors:  Alexandra C Graf; Peter Bauer; Ekkehard Glimm; Franz Koenig
Journal:  Biom J       Date:  2014-04-22       Impact factor: 2.207

3.  Flexible selection of a single treatment incorporating short-term endpoint information in a phase II/III clinical trial.

Authors:  Nigel Stallard; Cornelia Ursula Kunz; Susan Todd; Nicholas Parsons; Tim Friede
Journal:  Stat Med       Date:  2015-06-26       Impact factor: 2.373

4.  Planning multi-arm screening studies within the context of a drug development program.

Authors:  James M S Wason; Thomas Jaki; Nigel Stallard
Journal:  Stat Med       Date:  2013-03-26       Impact factor: 2.373

5.  A comparison of methods for treatment selection in seamless phase II/III clinical trials incorporating information on short-term endpoints.

Authors:  Cornelia Ursula Kunz; Tim Friede; Nicholas Parsons; Susan Todd; Nigel Stallard
Journal:  J Biopharm Stat       Date:  2015       Impact factor: 1.051

6.  Precision of maximum likelihood estimation in adaptive designs.

Authors:  Alexandra Christine Graf; Georg Gutjahr; Werner Brannath
Journal:  Stat Med       Date:  2015-10-12       Impact factor: 2.373

7.  Adaptive multiarm multistage clinical trials.

Authors:  Pranab Ghosh; Lingyun Liu; Cyrus Mehta
Journal:  Stat Med       Date:  2020-02-11       Impact factor: 2.373

8.  Data monitoring committees for clinical trials evaluating treatments of COVID-19.

Authors:  Tobias Mütze; Tim Friede
Journal:  Contemp Clin Trials       Date:  2020-09-19       Impact factor: 2.226

9.  Efficient Adaptive Designs for Clinical Trials of Interventions for COVID-19.

Authors:  Nigel Stallard; Lisa Hampson; Norbert Benda; Werner Brannath; Thomas Burnett; Tim Friede; Peter K Kimani; Franz Koenig; Johannes Krisam; Pavel Mozgunov; Martin Posch; James Wason; Gernot Wassmer; John Whitehead; S Faye Williamson; Sarah Zohar; Thomas Jaki
Journal:  Stat Biopharm Res       Date:  2020-07-29       Impact factor: 1.452

  9 in total

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