Background: In clinical trials, the opportunity for an early stop during an interim analysis (either for efficacy or for futility) may relevantly save time and financial resources. This is especially important, if the planning assumptions required for power calculation are based on a low level of evidence. For example, when including two primary endpoints in the confirmatory analysis, the power of the trial depends on the effects of both endpoints and on their correlation. Assessing the feasibility of such a trial is therefore difficult, as the number of parameter assumptions to be correctly specified is large. For this reason, so-called ‘group sequential designs’ are of particular importance in this setting. Whereas the choice of adequate ...
Introduction Most literature on optimal group-sequential designs focuses on minimising the expected ...
Background/Aims: Non-inferiority trials investigate whether a novel intervention, which typically ha...
Group sequential stopping rules are often used as guidelines in the monitoring of clinical trials in...
Abstract Background In clinical trials, the opportunity for an early stop during an interim analysis...
Background: In clinical trials with fixed study designs, statistical inference is only made when the...
This book focuses on group sequential methods for clinical trials with co-primary endpoints based on...
Group sequential design is widely used in today’s phase II/III clinical trials where testing multi...
Many different criteria have been proposed for the selection of a stopping rule for group sequen- ti...
This paper introduces a simple futility design that allows a comparative clinical trial to be stoppe...
BACKGROUND Randomised trial protocols may incorporate interim analyses, with the potential to sto...
Sequential methods provide a formal framework by which clinical trial data can be monitored as they ...
Graduation date: 2016Randomized trials are the gold standard for the clinical assessment of a new tr...
Background Assessing the long term effects of many surgical interventions tested in pragmatic RCTs ...
In classical group sequential designs, a clinical trial is considered as a success if the experiment...
Seamless phase II/III clinical trials in which an experimental treatment is selected at an interim a...
Introduction Most literature on optimal group-sequential designs focuses on minimising the expected ...
Background/Aims: Non-inferiority trials investigate whether a novel intervention, which typically ha...
Group sequential stopping rules are often used as guidelines in the monitoring of clinical trials in...
Abstract Background In clinical trials, the opportunity for an early stop during an interim analysis...
Background: In clinical trials with fixed study designs, statistical inference is only made when the...
This book focuses on group sequential methods for clinical trials with co-primary endpoints based on...
Group sequential design is widely used in today’s phase II/III clinical trials where testing multi...
Many different criteria have been proposed for the selection of a stopping rule for group sequen- ti...
This paper introduces a simple futility design that allows a comparative clinical trial to be stoppe...
BACKGROUND Randomised trial protocols may incorporate interim analyses, with the potential to sto...
Sequential methods provide a formal framework by which clinical trial data can be monitored as they ...
Graduation date: 2016Randomized trials are the gold standard for the clinical assessment of a new tr...
Background Assessing the long term effects of many surgical interventions tested in pragmatic RCTs ...
In classical group sequential designs, a clinical trial is considered as a success if the experiment...
Seamless phase II/III clinical trials in which an experimental treatment is selected at an interim a...
Introduction Most literature on optimal group-sequential designs focuses on minimising the expected ...
Background/Aims: Non-inferiority trials investigate whether a novel intervention, which typically ha...
Group sequential stopping rules are often used as guidelines in the monitoring of clinical trials in...