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Biometrics|March 27, 2010
Testing a primary and a secondary endpoint in a group sequential designAjit C Tamhane, Cyrus R Mehta, Lingyun LiuStatistics in Medicine|June 27, 2012
Adaptive extensions of a two-stage group sequential procedure for testing primary and secondary endpoints (II): sample size re-estimationAjit C Tamhane, Yi Wu, Cyrus R MehtaJournal of Biopharmaceutical Statistics|November 11, 2017
Penalty-based approaches to evaluating multiplicity adjustments in clinical trials: Advanced multiplicity problemsGautier Paux, Alex DmitrienkoStatistics in Medicine|October 12, 2013
Traditional multiplicity adjustment methods in clinical trialsAlex Dmitrienko, Ralph D'AgostinoJournal of Biopharmaceutical Statistics|November 28, 2017
Penalty-based approaches to evaluating multiplicity adjustments in clinical trials: Traditional multiplicity problemsGautier Paux, Alex DmitrienkoJournal of Biopharmaceutical Statistics|January 8, 2014
Strategies for identifying predictive biomarkers and subgroups with enhanced treatment effect in clinical trials using SIDESIlya Lipkovich, Alex DmitrienkoStatistics in Medicine|August 21, 2012
Superchain procedures in clinical trials with multiple objectivesGeorge Kordzakhia, Alex DmitrienkoBiometrics|June 8, 2017
A gatekeeping procedure to test a primary and a secondary endpoint in a group sequential design with multiple interim looksAjit C Tamhane, Jiangtao Gou, Christopher Jennison, et al.Statistics in Medicine|January 24, 2025
Testing One Primary and Two Secondary Endpoints in a Two-Stage Group Sequential Trial With ExtensionsAjit C Tamhane, Dong Xi, Cyrus R Mehta, et al.Journal of Biopharmaceutical Statistics|May 13, 2008
Sample size calculations in thorough QT studiesLu Zhang, Alex Dmitrienko, George LutaPageof 7