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Journal of Biopharmaceutical Statistics|June 1, 2005
Are we really that blind?Egbert A van der MeulenJournal of Biopharmaceutical Statistics|June 1, 2005
Sample size and power analysis for endometrial safety studiesGuoqin SuJournal of Biopharmaceutical Statistics|June 1, 2005
Performance of a mixed effects logistic regression model for binary outcomes with unequal cluster sizeMoonseong Heo, Andrew C LeonJournal of Biopharmaceutical Statistics|June 7, 2021
Four-parameter paired response curve for serial dilution assaysYouyi Fong, Sallie R Permar, Georgia D TomarasJournal of Biopharmaceutical Statistics|December 19, 2022
Comparison of profile-likelihood-based confidence intervals with other rank-based methods for the two-sample problem in ordered categorical dataIkuko Funatogawa, Takashi FunatogawaJournal of Biopharmaceutical Statistics|December 8, 2022
How to select the initial dose for a pediatric study?Jingjing Ye, Youwei Bi, Naitee TingJournal of Biopharmaceutical Statistics|January 6, 2023
Isotonic design for phase I cancer clinical trials with late-onset toxicitiesNolan A Wages, Thomas M Braun, Mark R ConawayJournal of Biopharmaceutical Statistics|January 13, 2023
Advancing drug development in pediatric oncology, a focus on cancer biology and targeted therapies: iMATRIX platformMarianne Uguen, Magalie Hilton, Mufiza Farid-Kapadia, et al.Journal of Biopharmaceutical Statistics|January 18, 2023
RESTART trial design: two-stage seamless transition design with operational considerationsMin Yi, Bin Zhuo, Freda CoonerJournal of Biopharmaceutical Statistics|June 24, 2021
Estimands and estimators of two-level methods using return to baseline strategy for longitudinal clinical trials with incomplete daily patient reported outcomesMan Jin, Guanghan LiuPageof 216