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20112025
most citedAn information-theoretic Phase I/II design for molecularly targeted agents that does not require an assumption of monotonicity

37 citations · 75 across the 30 of their papers we have counts for

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Showing 2020Show all

6 papers · 1 filter

stat.ME2020

A Novel Statistical Test for Treatment Differences in Clinical Trials using a Response Adaptive Forward Looking Gittins Index Rule

Helen Yvette Barnett, Sofia S Villar, Helena Geys +1

The most common objective for response adaptive clinical trials is to seek to ensure that patients within a trial have a high chance of receiving the best treatment available by al…

stat.ME2020★ 9 cited

Bayesian sample size determination using commensurate priors to leverage pre-experimental data

Haiyan Zheng, Thomas Jaki, James M. S. Wason

This paper develops Bayesian sample size formulae for experiments comparing two groups. We assume the experimental data will be analysed in the Bayesian framework, where pre-experi…

stat.AP2020

A Seamless Phase I/II Platform Design with a Time-To-Event Efficacy Endpoint for Potential COVID-19 Therapies

Thomas Jaki, Helen Barnett, Andrew Titman +1

In the search for effective treatments for COVID-19, initial emphasis has been on re-purposed treatments. To maximise the chances of finding successful treatments, novel treatments…

stat.AP2020★ 1 cited

Adding experimental treatment arms to Multi-Arm Multi-Stage platform trials in progress

Thomas Burnett, Franz König, Thomas Jaki

Multi-Arm Multi-Stage (MAMS) platform trials are an efficient tool for the comparison of several treatments. Suppose we wish to add a treatment to a trial already in progress, to a…

stat.AP2020

Adding flexibility to clinical trial designs: an example-based guide to the practical use of adaptive designs

Thomas Burnett, Pavel Mozgunov, Philip Pallmann +3

Adaptive designs for clinical trials permit alterations to a study in response to accumulating data in order to make trials more flexible, ethical and efficient. These benefits are…

stat.ME2020

Endpoints for randomized controlled clinical trials for COVID-19 treatments

Lori E Dodd, Dean Follmann, Jing Wang +12

Introduction: Endpoint choice for randomized controlled trials of treatments for COVID-19 is complex. A new disease brings many uncertainties, but trials must start rapidly. COVID-…