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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 2022Show all

5 papers · 1 filter

stat.ME2022

Point estimation for adaptive trial designs II: practical considerations and guidance

David S. Robertson, Babak Choodari-Oskooei, Munya Dimairo +3

In adaptive clinical trials, the conventional end-of-trial point estimate of a treatment effect is prone to bias, that is, a systematic tendency to deviate from its true value. As…

stat.ME2022★ 9 cited

Bayesian sample size determination in basket trials borrowing information between subsets

Haiyan Zheng, Michael J. Grayling, Pavel Mozgunov +2

Basket trials are increasingly used for the simultaneous evaluation of a new treatment in various patient subgroups under one overarching protocol. We propose a Bayesian approach t…

stat.AP2022★ 1 cited

Backfilling Cohorts in Phase I Dose-Escalation Studies

Helen Barnett, Oliver Boix, Dimitris Kontos +1

The use of `backfilling', assigning additional patients to doses deemed safe, in phase I dose-escalation studies has been used in practice to collect additional information on the…

stat.AP2022

Dose Finding Studies for Therapies with Late-Onset Safety and Efficacy Outcomes

Helen Barnett, Oliver Boix, Dimitris Kontos +1

In Phase I/II dose-finding trials, the objective is to find the Optimal Biological Dose (OBD), a dose that is both safe and efficacious that maximises some optimality criterion bas…

stat.ME2022★ 4 cited

Online error control for platform trials

David S. Robertson, James M. S. Wason, Franz König +2

Platform trials evaluate multiple experimental treatments under a single master protocol, where new treatment arms are added to the trial over time. Given the multiple treatment co…