Comparison of design strategies for a three-arm clinical trial with time-to-event endpoint: Power, time-to-analysis, and operational aspects-Reference-Cited by-同舟云学术

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Comparison of design strategies for a three-arm clinical trial with time-to-event endpoint: Power, time-to-analysis, and operational aspects

Published:2016-06-27 Issue:6 Volume:58 Page:1295-1310
ISSN:0323-3847
Container-title:Biometrical Journal
language:en
Short-container-title:Biom. J.

Author:

Asikanius Elina¹,Rufibach Kaspar¹,Bahlo Jasmin²,Bieska Gabriele¹,Burger Hans Ulrich¹

Affiliation:

1. F. Hoffmann-La Roche Ltd; Basel Switzerland

2. German CLL Study Group; Department I of Internal Medicine, University Hospital Cologne; Cologne Germany

Publisher

Wiley

Subject

Statistics, Probability and Uncertainty,General Medicine,Statistics and Probability

Reference38 articles.

1. Reporting of analyses from randomized controlled trials with multiple arms: a systematic review;Baron;BMC Medicine,2013

2. Twenty-five years of confirmatory adaptive designs: opportunities and pitfalls;Bauer;Statistics in Medicine,2016

3. Application of adaptive designs-a review;Bauer;Biometrical Journal,2006

4. Adaptive designs for confirmatory clinical trials;Bretz;Statistics in Medicine,2009

5. Confirmatory seamless phase II/III clinical trials with hypotheses selection at interim: general concepts;Bretz;Biometrical Journal,2006

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Blinded sample size recalculation in adaptive enrichment designs;Biometrical Journal;2022-08-19

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