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Journal of Biopharmaceutical Statistics|April 29, 2025
Application of complete N-of-1 trial design in bioequivalence-biosimilar drug developmentYuqing Liu, Wendy Lou, Shein-Chung ChowPharmaceutics|February 27, 2026
Switching Design for Assessment of Interchangeability in Biosimilar StudiesYuqing Liu, Wendy Lou, Shein-Chung ChowWiley Interdisciplinary Reviews. Computational Statistics|September 13, 2014
Bioavailability and Bioequivalence in Drug DevelopmentShein-Chung ChowControlled Clinical Trials|October 24, 2002
A note on statistical methods for assessing therapeutic equivalenceShein-Chung Chow, Jun ShaoJournal of Biopharmaceutical Statistics|February 18, 2020
Innovative design and analysis for rare disease drug developmentShein-Chung Chow, Zhipeng HuangTherapeutic Innovation & Regulatory Science|September 13, 2022
A Proposal for Post Hoc Subgroup Analysis in Support of Regulatory SubmissionJiajun Liu, Shein-Chung ChowStatistics in Medicine|December 14, 2005
On non-inferiority margin and statistical tests in active control trialsShein-Chung Chow, Jun ShaoJournal of Biopharmaceutical Statistics|July 19, 2005
Inference for clinical trials with some protocol amendmentsShein-Chung Chow, Jun ShaoOrphanet Journal of Rare Diseases|May 6, 2008
Adaptive design methods in clinical trials - a reviewShein-Chung Chow, Mark ChangPageof 99