Medical College of Wisconsin
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Optimal two-stage randomized phase II clinical trials. Clin Trials 2005;2(1):5-12 PMID: 16279574

Pubmed ID

16279574

Abstract

Randomized phase II clinical trials can be an efficient means of evaluating several potential new treatments prior to a comparative phase III clinical trial. However, selection designs do not allow for an assessment of minimal efficacy, nor do they allow early closing of a study arm for lack of efficacy, and so are only appropriate when all arms have met minimal efficacy requirements. Classic two-stage hypothesis testing based designs such as a Simon two-stage optimal design can satisfy these requirements, when used in parallel for the multiple treatment arms. However, these can be inefficient and impractical in terms of the maximum planned sample size required for such a study. This article proposes a two-stage randomized phase II clinical trial, where the sample size is adaptive at the second stage to the number of treatment arms passing through the first stage. The study design relies on optimality criteria, which are analogous to those used by Simon for single-arm studies. The proposed design maintains similar operating characteristics to a strategy of using multiple single-arm studies, in most situations of primary interest. Furthermore, it generally has smaller actual sample size when most of the treatments are effective than using multiple single-arm studies, leading to substantial efficiencies in terms of maximum planned sample size.

Author List

Logan BR

Author

Brent R. Logan PhD Director, Professor in the Institute for Health and Equity department at Medical College of Wisconsin




Scopus

2-s2.0-14744305954   6 Citations

MESH terms used to index this publication - Major topics in bold

Clinical Trials, Phase II as Topic
Data Interpretation, Statistical
Humans
Patient Selection
Randomized Controlled Trials as Topic
Research Design
Sample Size
Treatment Outcome
jenkins-FCD Prod-332 f92a19b0ec5e8e1eff783fac390ec127e367c2b5