Includes bibliographical references (p. 115-117).To save time and reduce the size and cost of clinical trials, surrogate endpoints are frequently measured instead of true endpoints. The proportion of the treatment effect explained by surrogate endpoints (PTE) is a widely used, albeit controversial, validation criteria. Frequentist and Bayesian methods have been developed to facilitate such validation. The former does not formally incorporate prior information; a critical issue since confidence intervals on PTE is often unacceptably wide. Both the Bayesian and frequentist approaches may yield estimates of PTE outside the unit interval. Furthermore, the existing Bayesian method offers no insight into the prior used for PTE, making prior-...
A common problem of interest within a randomized clinical trial is the evaluation of an inexpensive ...
Surrogate endpoints play an important role in drug development when they can be used to measure trea...
Exploratory analysis consumes much of the analysis effort in clinical trials, yet it is difficult to...
Surrogate endpoints are often used in clinical trials to serve as a substitute for a hard to achieve...
Surrogate endpoints are desirable in clinical trials when primary endpoints are costly to obtain, di...
This thesis considers a range of methodological challenges related to the trial-level validation of ...
The validation of surrogate endpoints has been studied by Prentice, who presented a definition as we...
A surrogate endpoint is intended to replace a clinical endpoint for the evaluation of new treatments...
We investigate the effect of the choice of parameterisation of meta-analytic models and related unce...
A number of meta-analytical methods have been proposed that aim to evaluate surrogate endpoints. Biv...
A number of meta-analytical methods have been proposed that aim to evaluate surrogate endpoints. Biv...
The predictive probability of success of a future clinical trial is a key quantitative tool for deci...
Surrogate endpoints play an important role in drug development when they can be used to measure trea...
A surrogate end point is often used to evaluate the effects of treatments or exposures on the true e...
In this paper, a Bayesian approach is developed for simultaneously comparing multiple experimental t...
A common problem of interest within a randomized clinical trial is the evaluation of an inexpensive ...
Surrogate endpoints play an important role in drug development when they can be used to measure trea...
Exploratory analysis consumes much of the analysis effort in clinical trials, yet it is difficult to...
Surrogate endpoints are often used in clinical trials to serve as a substitute for a hard to achieve...
Surrogate endpoints are desirable in clinical trials when primary endpoints are costly to obtain, di...
This thesis considers a range of methodological challenges related to the trial-level validation of ...
The validation of surrogate endpoints has been studied by Prentice, who presented a definition as we...
A surrogate endpoint is intended to replace a clinical endpoint for the evaluation of new treatments...
We investigate the effect of the choice of parameterisation of meta-analytic models and related unce...
A number of meta-analytical methods have been proposed that aim to evaluate surrogate endpoints. Biv...
A number of meta-analytical methods have been proposed that aim to evaluate surrogate endpoints. Biv...
The predictive probability of success of a future clinical trial is a key quantitative tool for deci...
Surrogate endpoints play an important role in drug development when they can be used to measure trea...
A surrogate end point is often used to evaluate the effects of treatments or exposures on the true e...
In this paper, a Bayesian approach is developed for simultaneously comparing multiple experimental t...
A common problem of interest within a randomized clinical trial is the evaluation of an inexpensive ...
Surrogate endpoints play an important role in drug development when they can be used to measure trea...
Exploratory analysis consumes much of the analysis effort in clinical trials, yet it is difficult to...