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Interim Monitoring for Futility in Clinical Trials With Two Co-Primary Endpoints Using Prediction

Version 2 2019-11-04, 22:35
Version 1 2019-10-08, 18:48
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posted on 2019-11-04, 22:35 authored by Koko Asakura, Scott R. Evans, Toshimitsu Hamasaki

We discuss using prediction as a flexible and practical approach for monitoring futility in clinical trials with two co-primary endpoints (CPE). This approach is appealing in that it provides quantitative evaluation of potential effect sizes and associated precision, and can be combined with flexible error-spending strategies. We extend prediction of effect size estimates and the construction of predicted intervals to the two CPE case, and illustrate interim futility monitoring of treatment effects using prediction with an example. We also discuss alternative approaches based on the conditional and predictive powers, compare these methods and provide some guidance on the use of prediction for better decision in clinical trials with CPE.

Funding

The research reported in this publication was supported by JSPS KAKENHI under grant numbers 15K15957 and 17K00069; the Japan Agency for Medical Research and Development under the Project Promoting Clinical Trials for Development of New Drugs 19lk0201061h0002 and 19lk0201061h0202; and the National Institute of Allergy and Infectious Diseases under award number UM1AI104681. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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