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Pharmaceutical Statistics|July 5, 2019
A comparison of subgroup identification methods in clinical drug development: Simulation study and regulatory considerationsCynthia Huber, Norbert Benda, Tim FriedePharmaceutical Statistics|March 15, 2022
The importance of using ordinal scores for patient classification based on health-related quality of life trajectoriesAntoine Barbieri, Florence Cousson-Gélie, Louise Baussard, et al.Pharmaceutical Statistics|January 13, 2023
Key considerations for choosing a statistical method to deal with incomplete treatment adherence in pragmatic trialsMd Belal Hossain, Mohammad Ehsanul KarimPharmaceutical Statistics|December 16, 2022
Parametric and nonparametric methods for confidence intervals and sample size planning for win probability in parallel-group randomized trials with Likert item and Likert scale dataGuangyong Zou, Lily Zou, Shi-Fang QiuPharmaceutical Statistics|January 5, 2023
A fiducial approach for testing the non-inferiority of proportion difference in matched-pairs designChao Chen, Siyang Ye, Jiahao Xu, et al.Pharmaceutical Statistics|November 10, 2010
Mixed models for data from thorough QT studies: part 2. One-step assessment of conditional QT prolongationRobert SchallPharmaceutical Statistics|November 10, 2010
Assessing non-inferiority to an aggregate response with an application to development of pneumococcal conjugate vaccinesYi Pan, Guanghan F Liu, Michael J DallasPharmaceutical Statistics|October 12, 2010
The role of the minimum clinically important difference and its impact on designing a trialChristy Chuang-Stein, Simon Kirby, Ian Hirsch, et al.Pharmaceutical Statistics|October 6, 2010
Issues for stratified randomization based on a factor derived from a continuous baseline variableYongming QuPharmaceutical Statistics|October 23, 2010
A course for clinical trial personnel in clinical study designs, randomization, allocation schedules, and interactive response systemsGregory T Golm, Thomas E Bradstreet, Laura A CoffeyPageof 120