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Journal of Biopharmaceutical Statistics|August 19, 2025
Evaluating bias in the anchor method for the minimal clinically important difference: a simulation approachGreg Hather, Polyna KhudyakovJournal of Biopharmaceutical Statistics|September 9, 2025
A bias correction method for hazard ratio estimation and its inference in a multiple-arm clinical trialLiji Shen, Ziwen Wei, Xuan DengJournal of Biopharmaceutical Statistics|September 9, 2025
Comparison of parametric and hybrid methods for estimating mean survival time in clinical studyYuki Nakagawa, Takashi SozuJournal of Biopharmaceutical Statistics|May 17, 2021
Incorporating propensity scores for evidence synthesis under bayesian framework: review and recommendations for clinical studiesJunjing Lin, Jianchang LinJournal of Biopharmaceutical Statistics|May 24, 2021
Evaluation of the lifetime performance index on first failure progressive censored data based on Topp Leone Alpha power exponential model applied on HPLC dataEl-Houssainy A Rady, Wafaa Hassanein, Shaimaa YehiaJournal of Biopharmaceutical Statistics|December 28, 2025
Covariate adjusted dose-response curves with applications to vaccine clinical trialsNong Shang, Stephanie Schrag, Rebecca Kahn, et al.Journal of Biopharmaceutical Statistics|December 22, 2025
Construction of multinomial distributions under mean constraints and its application in power analysesLin Fei, Changchun Xie, Md Monir HossainJournal of Biopharmaceutical Statistics|December 4, 2025
TITE-STEIN: Time-to-event simple toxicity and efficacy interval design to accelerate phase I/II trialsHao Sun, Jieqi Tu, Revathi Ananthakrishnan, et al.Journal of Biopharmaceutical Statistics|December 2, 2025
Estimands for long-term follow-up trials in gene therapy productsShihua Wen, Patricia Anderson, Ran Duan, et al.Journal of Biopharmaceutical Statistics|November 28, 2025
M-DODII: Bayesian dose optimization design for randomized phase II study with multiple indicationsSasha Amdur Kravets, Ziji Yu, Rachael Liu, et al.Pageof 216