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Statistics in Medicine
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June 21, 2012
Incorporating prognostic factors into causal estimators: a comparison of methods for randomised controlled trials with a time-to-event outcome
Lisa V Hampson, Chris Metcalfe
Biometrical Journal. Biometrische Zeitschrift
|
April 15, 2020
A Bayesian decision-theoretic approach to incorporate preclinical information into phase I oncology trials
Haiyan Zheng, Lisa V Hampson
Statistics in Medicine
|
October 13, 2015
Designing multi-arm multi-stage clinical trials using a risk-benefit criterion for treatment selection
Thomas Jaki, Lisa V Hampson
Statistics in Medicine
|
October 16, 2014
Optimizing the data combination rule for seamless phase II/III clinical trials
Lisa V Hampson, Christopher Jennison
Plos One
|
June 27, 2017
Many-to-one comparisons after safety selection in multi-arm clinical trials
Gerald Hlavin, Lisa V Hampson, Franz Koenig
Statistical Methods in Medical Research
|
January 17, 2019
A robust Bayesian meta-analytic approach to incorporate animal data into phase I oncology trials
Haiyan Zheng, Lisa V Hampson, Simon Wandel
Statistical Methods in Medical Research
|
January 27, 2021
Bridging across patient subgroups in phase I oncology trials that incorporate animal data
Haiyan Zheng, Lisa V Hampson, Thomas Jaki
Statistical Methods in Medical Research
|
March 20, 2016
Extrapolation of efficacy and other data to support the development of new medicines for children: A systematic review of methods
Ian Wadsworth, Lisa V Hampson, Thomas Jaki
Statistical Methods in Medical Research
|
February 14, 2020
Exposure-response modelling approaches for determining optimal dosing rules in children
Ian Wadsworth, Lisa V Hampson, Björn Bornkamp, et al.
Statistics in Medicine
|
June 25, 2014
Bayesian methods for the design and interpretation of clinical trials in very rare diseases
Lisa V Hampson, John Whitehead, Despina Eleftheriou, et al.
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of 4
Search research articles
Search
Showing results (1-10 of 37) with videos related to
Sort By:
Page
of 4
Statistics in Medicine
|
June 21, 2012
Incorporating prognostic factors into causal estimators: a comparison of methods for randomised controlled trials with a time-to-event outcome
Lisa V Hampson, Chris Metcalfe
Biometrical Journal. Biometrische Zeitschrift
|
April 15, 2020
A Bayesian decision-theoretic approach to incorporate preclinical information into phase I oncology trials
Haiyan Zheng, Lisa V Hampson
Statistics in Medicine
|
October 13, 2015
Designing multi-arm multi-stage clinical trials using a risk-benefit criterion for treatment selection
Thomas Jaki, Lisa V Hampson
Statistics in Medicine
|
October 16, 2014
Optimizing the data combination rule for seamless phase II/III clinical trials
Lisa V Hampson, Christopher Jennison
Plos One
|
June 27, 2017
Many-to-one comparisons after safety selection in multi-arm clinical trials
Gerald Hlavin, Lisa V Hampson, Franz Koenig
Statistical Methods in Medical Research
|
January 17, 2019
A robust Bayesian meta-analytic approach to incorporate animal data into phase I oncology trials
Haiyan Zheng, Lisa V Hampson, Simon Wandel
Statistical Methods in Medical Research
|
January 27, 2021
Bridging across patient subgroups in phase I oncology trials that incorporate animal data
Haiyan Zheng, Lisa V Hampson, Thomas Jaki
Statistical Methods in Medical Research
|
March 20, 2016
Extrapolation of efficacy and other data to support the development of new medicines for children: A systematic review of methods
Ian Wadsworth, Lisa V Hampson, Thomas Jaki
Statistical Methods in Medical Research
|
February 14, 2020
Exposure-response modelling approaches for determining optimal dosing rules in children
Ian Wadsworth, Lisa V Hampson, Björn Bornkamp, et al.
Statistics in Medicine
|
June 25, 2014
Bayesian methods for the design and interpretation of clinical trials in very rare diseases
Lisa V Hampson, John Whitehead, Despina Eleftheriou, et al.
Page
of 4