Decision Theoretic Designs for Phase II Clinical Trials with Multiple Outcomes
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Publication:4666685
DOI10.1111/j.0006-341X.1999.00971.xzbMath1059.62717WikidataQ40712207 ScholiaQ40712207MaRDI QIDQ4666685
Nigel Stallard, Peter F. Thall, John Whitehead
Publication date: 13 April 2005
Published in: Biometrics (Search for Journal in Brave)
optimal stoppingbackward inductionsequential procedureclinical trial designsafety and efficacy minotoring
Applications of statistics to biology and medical sciences; meta analysis (62P10) Bayesian problems; characterization of Bayes procedures (62C10) Optimal stopping in statistics (62L15)
Related Items (10)
Bayesian designs and the control of frequentist characteristics: A practical solution ⋮ Bayesian techniques for sample size determination in clinical trials: a short review ⋮ Bayesian Optimal Design for Phase II Screening Trials ⋮ Bayesian predictive monitoring with bivariate binary outcomes in phase II clinical trials ⋮ Ethical issues in oncology biostatistics ⋮ Bayesian randomized clinical trials: A decision-theoretic sequential design ⋮ Computer science and decision theory ⋮ Decision-Theoretic Designs for Pre-Phase II Screening Trials in Oncology ⋮ Seamlessly Expanding a Randomized Phase II Trial to Phase III ⋮ Decision-Theoretic Designs for Phase II Clinical Trials Allowing for Competing Studies
Cites Work
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- Incorporating Toxicity Considerations Into the Design of Two-Stage Phase II Clinical Trials
- Sample Size Determination for Phase II Clinical Trials Based on Bayesian Decision Theory
- Practical Bayesian Guidelines for Phase IIB Clinical Trials
- A Sample-Size-Optimal Bayesian Procedure for Sequential Pharmaceutical Trials
- Bivariate Sequential Designs for Phase II Trials
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