Background Adaptive model-based dose-finding designs have demonstrated advantages over traditional rule-based designs but have increased statistical complexity but uptake has been slow especially outside of cancer trials. TRAFIC is a multi-centre, early phase trial in rheumatoid arthritis incorporating a model-based design.Methods A Bayesian adaptive dose-finding phase I trial rolling into a single-arm, single-stage phase II trial. Model parameters for phase I were chosen via Monte Carlo simulation evaluating objective performance measures under clinically relevant scenarios and incorporated stopping rules for early termination. Potential designs were further calibrated utilising dose transition pathways.Discussion TRAFIC is an MRC-funded t...
Background: Early and intensive treatment is important to inducing remission and preventing joint da...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...
Abstract Background Adaptive model-based dose-finding designs have demonstrated advantages over trad...
Abstract Introduction: Rheumatoid Arthritis (RA) is a chronic inflammatory disorder that typically ...
We describe a dose escalation procedure for a combined phase I/II clinical trial. The procedure is b...
Background: Modern designs for dose-finding studies (e.g., model-based designs such as continual rea...
The design of phase I studies is often challenging, because of limited evidence to inform study prot...
The landscape of drug development in oncology has changed from conventional chemotherapies to molecu...
Early phase, or phase I and phase II, trials are the first step in testing new medicines that have b...
The development of a new drug is a major undertaking and it is important to consider carefully the k...
In oncology field, early phase clinical trial designs have attracted the interest of clinicians and ...
The development of a new drug is a major undertaking and it is important to consider carefully the k...
Abstract Background It is important to quantify the dose response for a drug in phase 2a clinical tr...
Dose escalation trials for identifying the maximum tolerable dose (MTD) is commonly considered in ph...
Background: Early and intensive treatment is important to inducing remission and preventing joint da...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...
Abstract Background Adaptive model-based dose-finding designs have demonstrated advantages over trad...
Abstract Introduction: Rheumatoid Arthritis (RA) is a chronic inflammatory disorder that typically ...
We describe a dose escalation procedure for a combined phase I/II clinical trial. The procedure is b...
Background: Modern designs for dose-finding studies (e.g., model-based designs such as continual rea...
The design of phase I studies is often challenging, because of limited evidence to inform study prot...
The landscape of drug development in oncology has changed from conventional chemotherapies to molecu...
Early phase, or phase I and phase II, trials are the first step in testing new medicines that have b...
The development of a new drug is a major undertaking and it is important to consider carefully the k...
In oncology field, early phase clinical trial designs have attracted the interest of clinicians and ...
The development of a new drug is a major undertaking and it is important to consider carefully the k...
Abstract Background It is important to quantify the dose response for a drug in phase 2a clinical tr...
Dose escalation trials for identifying the maximum tolerable dose (MTD) is commonly considered in ph...
Background: Early and intensive treatment is important to inducing remission and preventing joint da...
My dissertation work primarily focuses on Bayesian adaptive design for phase I and phase II clinical...
There are two practical challenges in the phase I clinical trial conduct: lack of transparency to ph...