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A web application for the design of multi-arm clinical trials

BMC cancer, 2020-01, Vol.20 (1), p.80-80, Article 80

2020

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Operational complexities in international clinical trials: a systematic review of challenges and proposed solutions

BMJ open, 2024-04, Vol.14 (4), p.e077132-e077132

2024

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Two-stage phase II oncology designs using short-term endpoints for early stopping

Statistical methods in medical research, 2017-08, Vol.26 (4), p.1671-1683

2017

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Optimal design for multi-arm multi-stage clinical trials

Trials, 2011-12, Vol.12 (S1), p.A4-A4, Article A4

2011

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Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia

BMC genetics, 2010-09, Vol.11, p.80

2010

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When is a two-stage single-arm trial efficient? An evaluation of the impact of outcome delay

European journal of cancer (1990), 2022-05, Vol.166, p.270-278

2022

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Point estimation following a two-stage group sequential trial

Statistical methods in medical research, 2023-02, Vol.32 (2), p.287-304

2023

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Employing a latent variable framework to improve efficiency in composite endpoint analysis

Statistical methods in medical research, 2021-03, Vol.30 (3), p.702-716

2021

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A hybrid approach to comparing parallel-group and stepped-wedge cluster-randomized trials with a continuous primary outcome when there is uncertainty in the intra-cluster correlation

Clinical trials (London, England), 2023-02, Vol.20 (1), p.59-70

2023

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A latent variable model for improving inference in trials assessing the effect of dose on toxicity and composite efficacy endpoints

Statistical methods in medical research, 2020-01, Vol.29 (1), p.230-242

2020

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Improving phase II oncology trials using best observed RECIST response as an endpoint by modelling continuous tumour measurements

Statistics in medicine, 2017-12, Vol.36 (29), p.4616-4626

2017

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A General Framework for Two-Stage Analysis of Genome-wide Association Studies and Its Application to Case-Control Studies

American journal of human genetics, 2012-05, Vol.90 (5), p.760-773

2012

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Optimal multistage designs for randomised clinical trials with continuous outcomes

Statistics in medicine, 2012-02, Vol.31 (4), p.301-312

2012

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Design of telehealth trials – Introducing adaptive approaches

International journal of medical informatics (Shannon, Ireland), 2014-12, Vol.83 (12), p.870-880

2014

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A review of statistical designs for improving the efficiency of phase II studies in oncology

Statistical methods in medical research, 2016-06, Vol.25 (3), p.1010-1021

2016

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Using continuous data on tumour measurements to improve inference in phase II cancer studies

Statistics in medicine, 2013-11, Vol.32 (26), p.4639-4650

2013

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Group sequential designs for stepped-wedge cluster randomised trials

Clinical trials (London, England), 2017-10, Vol.14 (5), p.507-517

2017

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Bayesian sample size determination using commensurate priors to leverage preexperimental data

Biometrics, 2023-06, Vol.79 (2), p.669-683

2023

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The choice of test in phase II cancer trials assessing continuous tumour shrinkage when complete responses are expected

Statistical methods in medical research, 2015-12, Vol.24 (6), p.909-919

2015

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Use of an embedded, micro-randomised trial to investigate non-compliance in telehealth interventions

Clinical trials (London, England), 2016-08, Vol.13 (4), p.417-424

2016

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Two‐stage penalized regression screening to detect biomarker–treatment interactions in randomized clinical trials

Biometrics, 2022-03, Vol.78 (1), p.141-150

2022

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Subgroup analyses in randomized controlled trials frequently categorized continuous subgroup information

Journal of clinical epidemiology, 2022-10, Vol.150, p.72-79

2022

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Sensitization of pancreatic cancer cells to radiation by cerium oxide nanoparticle-induced ROS production

Nanomedicine, 2013-05, Vol.9 (4), p.558-569

2013

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A web application for the design of multi-arm clinical trials

Operational complexities in international clinical trials: a systematic review of challenges and proposed solutions

Two-stage phase II oncology designs using short-term endpoints for early stopping

Extracorporeal photopheresis (ECP) in the treatment of chronic lung allograft dysfunction (CLAD): a prospective, multicentre, open-label, randomised controlled trial studying the addition of ECP to standard care in the treatment of bilateral lung transplant patients with CLAD (E-CLAD UK)

Optimal design for multi-arm multi-stage clinical trials

Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia

When is a two-stage single-arm trial efficient? An evaluation of the impact of outcome delay

Point estimation following a two-stage group sequential trial

Employing a latent variable framework to improve efficiency in composite endpoint analysis

A hybrid approach to comparing parallel-group and stepped-wedge cluster-randomized trials with a continuous primary outcome when there is uncertainty in the intra-cluster correlation

A latent variable model for improving inference in trials assessing the effect of dose on toxicity and composite efficacy endpoints

Improving phase II oncology trials using best observed RECIST response as an endpoint by modelling continuous tumour measurements

A General Framework for Two-Stage Analysis of Genome-wide Association Studies and Its Application to Case-Control Studies

Optimal multistage designs for randomised clinical trials with continuous outcomes

Design of telehealth trials – Introducing adaptive approaches

A review of statistical designs for improving the efficiency of phase II studies in oncology

Using continuous data on tumour measurements to improve inference in phase II cancer studies

Group sequential designs for stepped-wedge cluster randomised trials

Bayesian sample size determination using commensurate priors to leverage preexperimental data

The choice of test in phase II cancer trials assessing continuous tumour shrinkage when complete responses are expected

Use of an embedded, micro-randomised trial to investigate non-compliance in telehealth interventions

Two‐stage penalized regression screening to detect biomarker–treatment interactions in randomized clinical trials

Subgroup analyses in randomized controlled trials frequently categorized continuous subgroup information

Sensitization of pancreatic cancer cells to radiation by cerium oxide nanoparticle-induced ROS production

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