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Journal of Biopharmaceutical Statistics|October 1, 2020
Fast QLB algorithm and hypothesis tests in logistic model for ophthalmologic bilateral correlated dataYi-Qi Lin, Yu-Shun Zhang, Guo-Liang Tian, et al.Journal of Biopharmaceutical Statistics|September 30, 2020
Empirical weighted Bayesian tolerance intervalsHong TranJournal of Biopharmaceutical Statistics|February 13, 2019
R-TPI: rolling toxicity probability interval design to shorten the duration and maintain safety of phase I trialsWentian Guo, Yuan Ji, Daniel LiJournal of Biopharmaceutical Statistics|November 23, 2020
The Joint i3+3 (Ji3+3) design for phase I/II adoptive cell therapy clinical trialsXiaolei Lin, Yuan JiJournal of Biopharmaceutical Statistics|October 28, 2021
Do strict decision criteria hamper productivity in the pharmaceutical industry?Stig Johan WiklundJournal of Biopharmaceutical Statistics|February 17, 2016
Boundary problem in Simon's two-stage clinical trial designsGuogen Shan, John J Chen, Changxing MaJournal of Biopharmaceutical Statistics|February 17, 2016
Multiple comparisons with two controls for ordered categorical responsesPing Yang, Siu Hung Cheung, Wai-Yin PoonJournal of Biopharmaceutical Statistics|September 23, 2015
Tradeoff-based optimization criteria in clinical trials with multiple objectives and adaptive designsAlex Dmitrienko, Gautier Paux, Erik Pulkstenis, et al.Journal of Biopharmaceutical Statistics|September 16, 2015
The role of quantitative safety evaluation in regulatory decision making of drugsAloka G Chakravarty, Rima Izem, Stephine Keeton, et al.Journal of Biopharmaceutical Statistics|September 18, 2015
Practical designs for Phase I combination studies in oncologyNolan A Wages, Anastasia Ivanova, Olga MarchenkoPageof 216