| Publication | Date of Publication | Type |
|---|
Group-sequential designs with an externally-driven change of primary endpoint
Statistics in Medicine | 2026-02-18 | Paper |
A practical design for a dual-agent dose-escalation trial that incorporates pharmacokinetic data
Statistics in Medicine | 2025-11-07 | Paper |
Design of platform trials with a change in the control treatment arm
Biometrics | 2025-11-06 | Paper |
Flexible sequential designs for multi-arm clinical trials
Statistics in Medicine | 2025-09-18 | Paper |
Authors' reply to comments on ``Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs''
Statistics in Medicine | 2025-08-08 | Paper |
Estimation in AB/BA crossover trials with application to bioequivalence studies with incomplete and complete data designs
Statistics in Medicine | 2025-08-08 | Paper |
Planning multi-arm screening studies within the context of a drug development program
Statistics in Medicine | 2025-07-08 | Paper |
A quantitative framework to inform extrapolation decisions in children
Journal of the Royal Statistical Society. Series A. Statistics in Society | 2025-01-22 | Paper |
Group sequential designs for clinical trials when the maximum sample size is uncertain
Statistics in Medicine | 2025-01-02 | Paper |
Validation of predicted individual treatment effects in out of sample respondents
Statistics in Medicine | 2024-12-12 | Paper |
Recurrent events modelling of haemophilia bleeding events
Journal of the Royal Statistical Society. Series C. Applied Statistics | 2024-11-27 | Paper |
An information theoretic phase I--II design for molecularly targeted agents that does not require an assumption of monotonicity
Journal of the Royal Statistical Society. Series C. Applied Statistics | 2024-11-21 | Paper |
Subgroup analysis of treatment effects for misclassified biomarkers with time-to-event data
Journal of the Royal Statistical Society. Series C. Applied Statistics | 2024-11-21 | Paper |
Point estimation for adaptive trial designs. I: A methodological review
Statistics in Medicine | 2024-10-30 | Paper |
Dose finding studies for therapies with late-onset toxicities: a comparison study of designs
Statistics in Medicine | 2024-10-30 | Paper |
Practical implementation of the partial ordering continual reassessment method in a phase I combination-schedule dose-finding trial
Statistics in Medicine | 2024-10-30 | Paper |
An order restricted multi-arm multi-stage clinical trial design
Statistics in Medicine | 2024-10-29 | Paper |
Estimation of treatment effects following a sequential trial of multiple treatments
Statistics in Medicine | 2024-10-29 | Paper |
Improving safety of the continual reassessment method via a modified allocation rule
Statistics in Medicine | 2024-10-29 | Paper |
Optimizing subgroup selection in two-stage adaptive enrichment and umbrella designs
Statistics in Medicine | 2024-10-29 | Paper |
Online error rate control for platform trials
Statistics in Medicine | 2024-10-28 | Paper |
Point estimation for adaptive trial designs. II: Practical considerations and guidance
Statistics in Medicine | 2024-10-28 | Paper |
A Bayesian multi-arm multi-stage clinical trial design incorporating information about treatment ordering
Statistics in Medicine | 2024-10-28 | Paper |
Adding experimental treatment arms to multi-arm multi-stage platform trials in progress
Statistics in Medicine | 2024-10-14 | Paper |
A multi-arm multi-stage platform design that allows preplanned addition of arms while still controlling the family-wise error
Statistics in Medicine | 2024-10-14 | Paper |
A comparison of Bayesian information borrowing methods in basket trials and a novel proposal of modified exchangeability‐nonexchangeability method
Statistics in Medicine | 2024-03-04 | Paper |
Bayesian Sample Size Determination Using Commensurate Priors to Leverage Preexperimental Data
Biometrics | 2023-10-30 | Paper |
A novel statistical test for treatment differences in clinical trials using a response‐adaptive forward‐looking Gittins Index Rule
Biometrics | 2023-10-30 | Paper |
Generalisations of a Bayesian decision-theoretic randomisation procedure and the impact of delayed responses
Computational Statistics and Data Analysis | 2022-07-22 | Paper |
An Information Theoretic Approach for Selecting Arms in Clinical Trials
Journal of the Royal Statistical Society Series B: Statistical Methodology | 2022-07-08 | Paper |
An evaluation of the bootstrap for model validation in mixture models
Communications in Statistics. Simulation and Computation | 2022-06-28 | Paper |
Loss functions in restricted parameter spaces and their Bayesian applications
Journal of Applied Statistics | 2022-02-24 | Paper |
Using a dose-finding benchmark to quantify the loss incurred by dichotomization in phase II dose-ranging studies
Biometrical Journal | 2021-07-09 | Paper |
Assessing systemic drug exposure in repeated dose toxicity studies in the case of complete and incomplete sampling
Biometrical Journal | 2020-09-28 | Paper |
Instrumental variable estimation in semi-parametric additive hazards models
Biometrics | 2020-02-07 | Paper |
A flexible design for advanced phase I/II clinical trials with continuous efficacy endpoints
Biometrical Journal | 2020-02-03 | Paper |
A diagnostic tool for checking assumptions of regression mixture models
JP Journal of Biostatistics | 2019-12-05 | Paper |
Confidence regions for treatment effects in subgroups in biomarker stratified designs
Biometrical Journal | 2019-02-28 | Paper |
A Bayesian adaptive design for clinical trials in rare diseases
Computational Statistics and Data Analysis | 2018-08-14 | Paper |
| A review of the deterministic and diffusion approximations for stochastic chemical reaction networks | 2017-11-07 | Paper |
An information-theoretic approach for selecting arms in clinical trials
(available as arXiv preprint) | 2017-08-08 | Paper |
Loss Functions in Restricted Parameter Spaces and Their Bayesian Applications
(available as arXiv preprint) | 2017-06-07 | Paper |
Statistical evaluation of toxicological assays with zero or near-to-zero proportions or counts in the concurrent negative control group: a tutorial
JP Journal of Biostatistics | 2014-11-14 | Paper |
A hybrid method to estimate the minimum effective dose for monotone and non-monotone dose-response relationships
Biometrics | 2014-06-17 | Paper |
Simultaneous confidence intervals that are compatible with closed testing in adaptive designs
Biometrika | 2014-01-17 | Paper |
Using regression mixture models with non-normal data: examining an ordered polytomous approach
Journal of Statistical Computation and Simulation | 2013-11-15 | Paper |
A generalized Dunnett test for multi-arm multi-stage clinical studies with treatment selection
Biometrika | 2012-06-18 | Paper |
Symmetric maximum kernel likelihood estimation
Journal of Statistical Computation and Simulation | 2011-02-03 | Paper |
