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Journal of Biopharmaceutical Statistics|July 16, 2019
The i3+3 design for phase I clinical trialsMeizi Liu, Sue-Jane Wang, Yuan Ji
Journal of Biopharmaceutical Statistics|August 24, 2022
PMED: Optimal Bayesian Platform Trial Design with Multiple EndpointsTian He, Rachael Liu, Meizi Liu, et al.
Statistics in Medicine|February 8, 2025
DOD-SSR: An Adaptive Seamless Phase II/III Design With Dose Optimization Decision and Sample Size Re-estimationMeizi Liu, Jianchang Lin, Yefei Zhang, et al.
Statistics in Medicine|October 20, 2023
BEATS: Bayesian hybrid design with flexible sample size adaptation for time-to-event endpointsDehua Bi, Meizi Liu, Jianchang Lin, et al.
Statistics in Medicine|June 14, 2021
Propensity-score-based meta-analytic predictive prior for incorporating real-world and historical dataMeizi Liu, Veronica Bunn, Bradley Hupf, et al.
Journal of Hazardous Materials|October 4, 2023
Flow cytometry-based high-throughput screening of synthetic peptides for palladium adsorptionLing Tan, Meizi Liu, Lixian Wang, et al.
Journal of Biopharmaceutical Statistics|March 12, 2024
DOD-Combo: Bayesian dose finding design in combination trials with meta-analytic-predictive priorKai Chen, Yunqi Zhao, Meizi Liu, et al.
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