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Pharmaceutical Statistics|December 13, 2022
A Bayesian method for safety signal detection in ongoing blinded randomised controlled trialsKristian Brock, Chen Chen, Shuyen Ho, et al.Pharmaceutical Statistics|May 10, 2022
A practical guide to sample size calculations: Installation of the app SampSizeLaura Flight, Steven A JuliousPharmaceutical Statistics|July 7, 2021
Adjusting for covariates in analysis based on restricted mean survival timesYi Zhong, Ou Zhao, Bo Zhang, et al.Pharmaceutical Statistics|September 16, 2020
Assessing the quality of studies in meta-research: Review/guidelines on the most important quality assessment toolsClaudio Luchini, Nicola Veronese, Alessia Nottegar, et al.Pharmaceutical Statistics|June 17, 2016
Hyperbaric oxygen brain injury treatment (HOBIT) trial: a multifactor design with response adaptive randomization and longitudinal modelingByron J Gajewski, Scott M Berry, William G Barsan, et al.Pharmaceutical Statistics|April 6, 2020
Improving interim decisions in randomized trials by exploiting information on short-term endpoints and prognostic baseline covariatesKelly Van Lancker, An Vandebosch, Stijn VansteelandtPharmaceutical Statistics|September 2, 2020
Cancer immunotherapy trial design with long-term survivorsXue Ding, Jianrong WuPharmaceutical Statistics|December 18, 2020
A confidence function-based posterior probability design for phase II cancer trialsMinghua ShanPharmaceutical Statistics|December 21, 2020
Sample size calculations for single-arm survival studies using transformations of the Kaplan-Meier estimatorKengo Nagashima, Hisashi Noma, Yasunori Sato, et al.Pharmaceutical Statistics|July 14, 2021
Identifying treatment effect heterogeneity in dose-finding trials using Bayesian hierarchical models: Identifying treatment effect heterogeneity in dose-finding trialsMarius Thomas, Björn Bornkamp, Katja IckstadtPageof 120