We consider the problem of how to efficiently and safely design dose finding studies. Both current and novel utility functions are explored using Bayesian adaptive design methodology for the estimation of a maximum tolerated dose (MTD). In particular, we explore widely adopted approaches such as the continual reassessment method and minimizing the variance of the estimate of an MTD. New utility functions are constructed in the Bayesian framework and are evaluated against current approaches. To reduce computing time, importance sampling is implemented to re-weight posterior samples thus avoiding the need to draw samples using Markov chain Monte Carlo techniques. Further, as such studies are generally first-in-man, the safety of patients is p...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
A Bayesian adaptive design is proposed for dose-finding in phase I/II clinical trials to incorporate...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...
In oncology, dose escalation is often carried out to search for the maximum tolerated dose (MTD) in ...
The primary objective of phase I dose-finding trials is to determine the maximum tolerated dose (MTD...
Improving methodology for Phase I dose-finding studies is currently of great interest in pharmaceuti...
We present a Bayesian adaptive design for dose finding of a combination of two drugs in cancer phase...
In this research, two new designs in clinical trials are proposed. The first problem is a new Bayesi...
In this research, two new designs in clinical trials are proposed. The first problem is a new Bayesi...
In this research, two new designs in clinical trials are proposed. The first problem is a new Bayesi...
Includes bibliographical references (p. 123-128).The process of conducting a pharmaceutical clinical...
Adaptive trial designs can considerably improve upon traditional designs, by modifying design aspect...
We present a Bayesian adaptive design for dose finding of a combination of two drugs in cancer phase...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
A Bayesian adaptive design is proposed for dose-finding in phase I/II clinical trials to incorporate...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...
In oncology, dose escalation is often carried out to search for the maximum tolerated dose (MTD) in ...
The primary objective of phase I dose-finding trials is to determine the maximum tolerated dose (MTD...
Improving methodology for Phase I dose-finding studies is currently of great interest in pharmaceuti...
We present a Bayesian adaptive design for dose finding of a combination of two drugs in cancer phase...
In this research, two new designs in clinical trials are proposed. The first problem is a new Bayesi...
In this research, two new designs in clinical trials are proposed. The first problem is a new Bayesi...
In this research, two new designs in clinical trials are proposed. The first problem is a new Bayesi...
Includes bibliographical references (p. 123-128).The process of conducting a pharmaceutical clinical...
Adaptive trial designs can considerably improve upon traditional designs, by modifying design aspect...
We present a Bayesian adaptive design for dose finding of a combination of two drugs in cancer phase...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
A Bayesian adaptive design is proposed for dose-finding in phase I/II clinical trials to incorporate...