Literature DB >> 9544519

An optimal design for screening trials.

Y G Wang1, D H Leung.   

Abstract

Yao, Begg, and Livingston (1996, Biometrics 52, 992-1001) considered the optimal group size for testing a series of potentially therapeutic agents to identify a promising one as soon as possible for given error rates. The number of patients to be tested with each agent was fixed as the group size. We consider a sequential design that allows early acceptance and rejection, and we provide an optimal strategy to minimize the sample sizes (patients) required using Markov decision processes. The minimization is under the constraints of the two types (false positive and false negative) of error probabilities, with the Lagrangian multipliers corresponding to the cost parameters for the two types of errors. Numerical studies indicate that there can be a substantial reduction in the number of patients required.

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Year:  1998        PMID: 9544519

Source DB:  PubMed          Journal:  Biometrics        ISSN: 0006-341X            Impact factor:   2.571


  2 in total

1.  Bayesian adaptive phase II screening design for combination trials.

Authors:  Chunyan Cai; Ying Yuan; Valen E Johnson
Journal:  Clin Trials       Date:  2013-01-28       Impact factor: 2.486

2.  Bayesian optimal design for phase II screening trials.

Authors:  Meichun Ding; Gary L Rosner; Peter Müller
Journal:  Biometrics       Date:  2007-12-20       Impact factor: 1.701

  2 in total

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