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Rui Sammi Tang

Showing results (1-10 of 13) with videos related to

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Statistics in Medicine|October 6, 2022
A proper statistical inference framework to compare clinical trial and real-world progression-free survival dataJian Zhu, Rui Sammi Tang
Journal of Biopharmaceutical Statistics|April 23, 2025
An improved biomarker-guided adaptive patient enrichment design for oncology trialsZhenwei Zhou, Zhaoyang Teng, Jian Zhu, et al.
Biometrics|May 13, 2022
A Bayesian platform trial design to simultaneously evaluate multiple drugs in multiple indications with mixed endpointsYujie Zhao, Rui Sammi Tang, Yeting Du, et al.
Biometrics|September 10, 2024
A Bayesian latent-subgroup platform design for dose optimizationRongji Mu, Xiaojiang Zhan, Rui Sammi Tang, et al.
Journal of Biopharmaceutical Statistics|January 31, 2022
Bayesian Divide-and-Conquer Propensity Score Based Approaches for Leveraging Real World Data in Single Arm Clinical TrialsEric Baron, Jian Zhu, Rui Sammi Tang, et al.
Statistics in Medicine|November 3, 2021
A Bayesian phase I/II platform design for co-developing drug combination therapies for multiple indicationsRongji Mu, Jin Xu, Rui Sammi Tang, et al.
Statistics in Medicine|November 25, 2025
Bayesian Prediction of Event Times Using Mixture Model for Blinded Randomized Controlled TrialsJingyan Fu, Dan Zhao, Donia Skanji, et al.
JCO Precision Oncology|December 22, 2025
Master Protocol Design With Hybrid Control for Efficient Early-Phase Trial ConsolidationAlexander M Kaizer, Xiaojiang Zhan, Eric Baron, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|June 29, 2017
Special Issue: Selected Papers of the Inaugural DahShu Data Science Symposium: Computational Precision Health (CPH 2017)Haiyan Huang, Hua Tang, Jing Huang, et al.
Contemporary Clinical Trials|March 25, 2022
Impact of COVID-19 pandemic on oncology clinical trial design, data collection and analysisRui Sammi Tang, Jian Zhu, Tai-Tsang Chen, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Statistics in Medicine|October 6, 2022
A proper statistical inference framework to compare clinical trial and real-world progression-free survival dataJian Zhu, Rui Sammi Tang
Journal of Biopharmaceutical Statistics|April 23, 2025
An improved biomarker-guided adaptive patient enrichment design for oncology trialsZhenwei Zhou, Zhaoyang Teng, Jian Zhu, et al.
Biometrics|May 13, 2022
A Bayesian platform trial design to simultaneously evaluate multiple drugs in multiple indications with mixed endpointsYujie Zhao, Rui Sammi Tang, Yeting Du, et al.
Biometrics|September 10, 2024
A Bayesian latent-subgroup platform design for dose optimizationRongji Mu, Xiaojiang Zhan, Rui Sammi Tang, et al.
Journal of Biopharmaceutical Statistics|January 31, 2022
Bayesian Divide-and-Conquer Propensity Score Based Approaches for Leveraging Real World Data in Single Arm Clinical TrialsEric Baron, Jian Zhu, Rui Sammi Tang, et al.
Statistics in Medicine|November 3, 2021
A Bayesian phase I/II platform design for co-developing drug combination therapies for multiple indicationsRongji Mu, Jin Xu, Rui Sammi Tang, et al.
Statistics in Medicine|November 25, 2025
Bayesian Prediction of Event Times Using Mixture Model for Blinded Randomized Controlled TrialsJingyan Fu, Dan Zhao, Donia Skanji, et al.
JCO Precision Oncology|December 22, 2025
Master Protocol Design With Hybrid Control for Efficient Early-Phase Trial ConsolidationAlexander M Kaizer, Xiaojiang Zhan, Eric Baron, et al.
Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|June 29, 2017
Special Issue: Selected Papers of the Inaugural DahShu Data Science Symposium: Computational Precision Health (CPH 2017)Haiyan Huang, Hua Tang, Jing Huang, et al.
Contemporary Clinical Trials|March 25, 2022
Impact of COVID-19 pandemic on oncology clinical trial design, data collection and analysisRui Sammi Tang, Jian Zhu, Tai-Tsang Chen, et al.
Pageof 2