This paper introduces a simple futility design that allows a comparative clinical trial to be stopped due to lack of effect at any of a series of planned interim analyses. Stopping due to apparent benefit is not permitted. The design is for use when any positive claim should be based on the maximum sample size, for example to allow subgroup analyses or the evaluation of safety or secondary efficacy responses. A final frequentist analysis can be performed that is valid for the type of design employed. Here the design is described and its properties are presented. Its advantages and disadvantages relative to the use of stochastic curtailment are discussed. Copyright (C) 2003 John Wiley Sons, Ltd
Abstract background The pace of novel medical treatments and approaches to therapy has accelerated i...
As part of the drug development process, interim analysis is frequently used to design efficient pha...
Sequential methods provide a formal framework by which clinical trial data can be monitored as they ...
Abstract Background In clinical trials, the opportunity for an early stop during an interim analysis...
BACKGROUND: Many clinical trials show no overall benefit. We examined futility analyses applied to t...
Two-stage designs that allow for early stopping if the treatment is ineffective are commonly used in...
Background: In clinical trials with fixed study designs, statistical inference is only made when the...
Group sequential stopping rules are often used as guidelines in the monitoring of clinical trials in...
Background Publicly funded trials regularly fail to recruit their target sample size or find a si...
Many different criteria have been proposed for the selection of a stopping rule for group sequen- ti...
Randomised controlled trials are considered the gold standard in trial design. However, phase II onc...
Phase II clinical trials are a critical aspect of the drug development process. With drug developmen...
Interim analysis is important in a large clinical trial for ethical and cost considerations. Sometim...
This book focuses on group sequential methods for clinical trials with co-primary endpoints based on...
Designs incorporating more than one endpoint have become popular in drug development. One of such de...
Abstract background The pace of novel medical treatments and approaches to therapy has accelerated i...
As part of the drug development process, interim analysis is frequently used to design efficient pha...
Sequential methods provide a formal framework by which clinical trial data can be monitored as they ...
Abstract Background In clinical trials, the opportunity for an early stop during an interim analysis...
BACKGROUND: Many clinical trials show no overall benefit. We examined futility analyses applied to t...
Two-stage designs that allow for early stopping if the treatment is ineffective are commonly used in...
Background: In clinical trials with fixed study designs, statistical inference is only made when the...
Group sequential stopping rules are often used as guidelines in the monitoring of clinical trials in...
Background Publicly funded trials regularly fail to recruit their target sample size or find a si...
Many different criteria have been proposed for the selection of a stopping rule for group sequen- ti...
Randomised controlled trials are considered the gold standard in trial design. However, phase II onc...
Phase II clinical trials are a critical aspect of the drug development process. With drug developmen...
Interim analysis is important in a large clinical trial for ethical and cost considerations. Sometim...
This book focuses on group sequential methods for clinical trials with co-primary endpoints based on...
Designs incorporating more than one endpoint have become popular in drug development. One of such de...
Abstract background The pace of novel medical treatments and approaches to therapy has accelerated i...
As part of the drug development process, interim analysis is frequently used to design efficient pha...
Sequential methods provide a formal framework by which clinical trial data can be monitored as they ...