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Pharmaceutical Statistics|October 7, 2010
Optimal caliper widths for propensity-score matching when estimating differences in means and differences in proportions in observational studiesPeter C AustinPharmaceutical Statistics|October 23, 2010
Review of the statistical analysis of the dog telemetry studyMike Aylott, Simon Bate, Susie Collins, et al.Pharmaceutical Statistics|August 26, 2010
Practical issues and lessons learned from multi-regional clinical trials via case examples: a Japanese perspectiveYuki Ando, Toshimitsu HamasakiPharmaceutical Statistics|February 11, 2011
Additional results for 'Sequential design approaches for bioequivalence studies with crossover designs'Timothy H Montague, Diane Potvin, Charles E Diliberti, et al.Pharmaceutical Statistics|January 27, 2011
A new mathematical approach for the estimation of the AUC and its variability under different experimental designs in preclinical studiesCarmen Navarro-Fontestad, Isabel González-Álvarez, Carlos Fernández-Teruel, et al.Pharmaceutical Statistics|June 23, 2010
Proposals of statistical consideration to evaluation of results for a specific region in multi-regional trials--Asian perspectiveHsiao-Hui Tsou, Shein-Chung Chow, K K Gordon Lan, et al.Pharmaceutical Statistics|January 29, 2011
Making available information from studies sponsored by the pharmaceutical industry: some current practicesMichael O'Kelly, Steven A Julious, Stephen Pyke, et al.Pharmaceutical Statistics|March 24, 2021
A simulation-free group sequential design with max-combo tests in the presence of non-proportional hazardsLili Wang, Xiaodong Luo, Cheng ZhengPharmaceutical Statistics|December 1, 2021
The power prior with multiple historical controls for the linear regression modelAkalu Banbeta, Emmanuel Lesaffre, Joost van RosmalenPharmaceutical Statistics|July 17, 2019
Random effects models for estimation of the probability and time to progression of a continuous biomarkerTarylee Reddy, Geert Molenberghs, Liesbeth Bruckers, et al.Pageof 119