The motivation for the work in this article is the setting in which a number of treatments are available for evaluation in phase II clinical trials and where it may be infeasible to try them concurrently because the intended population is small. This paper introduces an extension of previous work on decision-theoretic designs for a series of phase II trials. The program encompasses a series of sequential phase II trials with interim decision making and a single two-arm phase III trial. The design is based on a hybrid approach where the final analysis of the phase III data is based on a classical frequentist hypothesis test, whereas the trials are designed using a Bayesian decision-theoretic approach in which the unknown treatment effect is ...
Early phase, or phase I and phase II, trials are the first step in testing new medicines that have b...
This paper considers the design and interpretation of clinical trials comparing treatments for condi...
Background/Aims: Combinations of treatments that have already received regulatory approval can offer...
Background: Adaptive designs offer added flexibility in the execution of clinical trials, including ...
Pilot studies and other small clinical trials are often conducted but serve a variety of purposes an...
Background Adaptive designs offer added flexibility in the execution of clinical tri...
Background: Phase III trials often require large sample sizes, leading to high costs and delays in ...
This paper introduces a decision-theoretic design for a series of phase II trials. Instead of design...
BACKGROUND Phase III trials often require large sample sizes, leading to high costs and delays in...
Randomised controlled trials are considered the gold standard in trial design. However, phase II onc...
<div><p>Single-arm studies are typically used in phase II of clinical trials, whose main objective i...
Recent scientific advances in biomedical research have rapidly increased the number of promising new...
Rapid progress in biomedical research necessitates clinical evaluation that identifies promising inn...
Properly planned and executed clinical trials play a vital role for modern medicine. They have been ...
This thesis presents designs for a series of clinical trials where instead of designing clinical tri...
Early phase, or phase I and phase II, trials are the first step in testing new medicines that have b...
This paper considers the design and interpretation of clinical trials comparing treatments for condi...
Background/Aims: Combinations of treatments that have already received regulatory approval can offer...
Background: Adaptive designs offer added flexibility in the execution of clinical trials, including ...
Pilot studies and other small clinical trials are often conducted but serve a variety of purposes an...
Background Adaptive designs offer added flexibility in the execution of clinical tri...
Background: Phase III trials often require large sample sizes, leading to high costs and delays in ...
This paper introduces a decision-theoretic design for a series of phase II trials. Instead of design...
BACKGROUND Phase III trials often require large sample sizes, leading to high costs and delays in...
Randomised controlled trials are considered the gold standard in trial design. However, phase II onc...
<div><p>Single-arm studies are typically used in phase II of clinical trials, whose main objective i...
Recent scientific advances in biomedical research have rapidly increased the number of promising new...
Rapid progress in biomedical research necessitates clinical evaluation that identifies promising inn...
Properly planned and executed clinical trials play a vital role for modern medicine. They have been ...
This thesis presents designs for a series of clinical trials where instead of designing clinical tri...
Early phase, or phase I and phase II, trials are the first step in testing new medicines that have b...
This paper considers the design and interpretation of clinical trials comparing treatments for condi...
Background/Aims: Combinations of treatments that have already received regulatory approval can offer...