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Journal of Biopharmaceutical Statistics|September 8, 2020
Enhancing clarity of clinical trial safety reports for data monitoring committeesSonia M Thomas, Kwanhye Jung, Hengrui Sun, et al.Journal of Biopharmaceutical Statistics|September 15, 2020
A simulation study of approaches for handling disease progression in dose-finding clinical trialsLucie Biard, Bin Cheng, Gulam A Manji, et al.Journal of Biopharmaceutical Statistics|September 3, 2020
Baseline selection in concentration-QTc modeling: impact on assay sensitivityDalong Patrick Huang, Janell Chen, Yi TsongJournal of Biopharmaceutical Statistics|September 29, 2020
Multiplicity issues for platform trials with a shared control armXiaofei Bai, Qiqi Deng, Dacheng LiuJournal of Biopharmaceutical Statistics|September 29, 2020
Power calculations for the sequential parallel comparison design with continuous outcomesAnastasia Ivanova, Bahjat QaqishJournal of Biopharmaceutical Statistics|March 5, 2020
Two-stage optimal designs based on exact variance for a single-arm trial with survival endpointsGuogen ShanJournal of Biopharmaceutical Statistics|March 5, 2020
Bayesian Semi-parametric Design (BSD) for adaptive dose-finding with multiple strataMo Li, Rachael Liu, Jianchang Lin, et al.Journal of Biopharmaceutical Statistics|March 5, 2020
Estimation of the area under a curve via several B-spline-based regression methods and applicationsMingmei Tian, Jihnhee Yu, Joonyeong KimJournal of Biopharmaceutical Statistics|February 13, 2019
Approaches for testing noninferiority in two-arm trials for risk ratio and odds ratioShrabanti Chowdhury, Ram C Tiwari, Samiran GhoshJournal of Biopharmaceutical Statistics|February 13, 2019
Semi-parametric Bayesian regression for subgroup analysis in clinical trialsMargaret Gamalo-Siebers, Ram TiwariPageof 219