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Statistics in Medicine
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May 19, 2016
Utility-based designs for randomized comparative trials with categorical outcomes
Thomas A Murray, Peter F Thall, Ying Yuan
Journal of the Royal Statistical Society. Series C, Applied Statistics
|
April 2, 2016
Bayesian Group Sequential Clinical Trial Design using Total Toxicity Burden and Progression-Free Survival
Brian P Hobbs, Peter F Thall, Steven H Lin
Journal of the Royal Statistical Society. Series C, Applied Statistics
|
March 4, 2017
Parametric Dose Standardization for Optimizing Two-Agent Combinations in a Phase I-II Trial with Ordinal Outcomes
Peter F Thall, Hoang Q Nguyen, Ralph G Zinner
Pharmaceutical Statistics
|
July 6, 2017
Bayesian nonparametric statistics: A new toolkit for discovery in cancer research
Peter F Thall, Peter Mueller, Yanxun Xu, et al.
Journal of the American Statistical Association
|
September 15, 2015
Bayesian Dose-Finding in Two Treatment Cycles Based on the Joint Utility of Efficacy and Toxicity
Juhee Lee, Peter F Thall, Yuan Ji, et al.
Biostatistics (Oxford, England)
|
November 11, 2015
A decision-theoretic phase I-II design for ordinal outcomes in two cycles
Juhee Lee, Peter F Thall, Yuan Ji, et al.
Clinical Trials (London, England)
|
January 21, 2006
Monitoring event times in early phase clinical trials: some practical issues
Peter F Thall, Leiko H Wooten, Nizar M Tannir
Biometrics
|
October 3, 2024
ROMI: a randomized two-stage basket trial design to optimize doses for multiple indications
Shuqi Wang, Peter F Thall, Kentaro Takeda, et al.
Statistics in Medicine
|
June 23, 2015
Optimization of multi-stage dynamic treatment regimes utilizing accumulated data
Xuelin Huang, Sangbum Choi, Lu Wang, et al.
Journal of Biopharmaceutical Statistics
|
October 14, 2006
Adaptive dose selection using efficacy-toxicity trade-offs: illustrations and practical considerations
Peter F Thall, John D Cook, Elihu H Estey
Page
of 19
Search research articles
Search
Showing results (51-60 of 190) with videos related to
Sort By:
Page
of 19
Statistics in Medicine
|
May 19, 2016
Utility-based designs for randomized comparative trials with categorical outcomes
Thomas A Murray, Peter F Thall, Ying Yuan
Journal of the Royal Statistical Society. Series C, Applied Statistics
|
April 2, 2016
Bayesian Group Sequential Clinical Trial Design using Total Toxicity Burden and Progression-Free Survival
Brian P Hobbs, Peter F Thall, Steven H Lin
Journal of the Royal Statistical Society. Series C, Applied Statistics
|
March 4, 2017
Parametric Dose Standardization for Optimizing Two-Agent Combinations in a Phase I-II Trial with Ordinal Outcomes
Peter F Thall, Hoang Q Nguyen, Ralph G Zinner
Pharmaceutical Statistics
|
July 6, 2017
Bayesian nonparametric statistics: A new toolkit for discovery in cancer research
Peter F Thall, Peter Mueller, Yanxun Xu, et al.
Journal of the American Statistical Association
|
September 15, 2015
Bayesian Dose-Finding in Two Treatment Cycles Based on the Joint Utility of Efficacy and Toxicity
Juhee Lee, Peter F Thall, Yuan Ji, et al.
Biostatistics (Oxford, England)
|
November 11, 2015
A decision-theoretic phase I-II design for ordinal outcomes in two cycles
Juhee Lee, Peter F Thall, Yuan Ji, et al.
Clinical Trials (London, England)
|
January 21, 2006
Monitoring event times in early phase clinical trials: some practical issues
Peter F Thall, Leiko H Wooten, Nizar M Tannir
Biometrics
|
October 3, 2024
ROMI: a randomized two-stage basket trial design to optimize doses for multiple indications
Shuqi Wang, Peter F Thall, Kentaro Takeda, et al.
Statistics in Medicine
|
June 23, 2015
Optimization of multi-stage dynamic treatment regimes utilizing accumulated data
Xuelin Huang, Sangbum Choi, Lu Wang, et al.
Journal of Biopharmaceutical Statistics
|
October 14, 2006
Adaptive dose selection using efficacy-toxicity trade-offs: illustrations and practical considerations
Peter F Thall, John D Cook, Elihu H Estey
Page
of 19