Works by Chow, Shein-Chung
Results: 179
Novel Design and Analysis for Rare Disease Drug Development.
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- Mathematics (2227-7390), 2024, v. 12, n. 5, p. 631, doi. 10.3390/math12050631
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- Article
Authors' reply to the letter to the editor by L. Chen and Y. X. Liu.
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- Pharmaceutical Statistics, 2012, v. 11, n. 4, p. 343, doi. 10.1002/pst.1518
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- Article
Assessing departure from dose linearity under a repeated measures incomplete block design.
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- Pharmaceutical Statistics, 2011, v. 10, n. 4, p. 357, doi. 10.1002/pst.474
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- Article
Proposals of statistical consideration to evaluation of results for a specific region in multi-regional trials - Asian perspective.
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- Pharmaceutical Statistics, 2010, v. 9, n. 3, p. 201, doi. 10.1002/pst.442
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- Article
Inference on treatment effects for targeted clinical trials under enrichment design.
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- Pharmaceutical Statistics, 2009, v. 8, n. 4, p. 356, doi. 10.1002/pst.364
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- Article
Use of left atrial appendage occlusion among older cardiac surgery patients with preoperative atrial fibrillation: a national cohort study.
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- 2020
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- journal article
Efficacy of Transcendental Meditation to Reduce Stress Among Health Care Workers: A Randomized Clinical Trial.
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- JAMA Network Open, 2022, v. 5, n. 9, p. e2231917, doi. 10.1001/jamanetworkopen.2022.31917
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- Article
Ovarian reserve diminished by oral cyclophosphamide therapy for granulomatosis with polyangiitis (Wegener's).
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- Arthritis Care & Research, 2011, v. 63, n. 12, p. 1777, doi. 10.1002/acr.20605
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- Article
Statistical and regulatory considerations in assessments of interchangeability of biological drug products.
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- European Journal of Health Economics, 2014, v. 15, p. 5, doi. 10.1007/s10198-014-0589-1
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- Article
Sequential Adaptive Design Method for Incorporating External Data.
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- Biometrical Journal, 2024, v. 66, n. 8, p. 1, doi. 10.1002/bimj.70003
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- Article
Empower clinical development by harnessing data from diverse sources: methodology, applications and regulatory perspectives.
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- Journal of Biopharmaceutical Statistics, 2024, v. 34, n. 6, p. 775, doi. 10.1080/10543406.2024.2333529
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- Article
Utility of real-world evidence in biosimilar development.
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- Journal of Biopharmaceutical Statistics, 2024, v. 34, n. 6, p. 842, doi. 10.1080/10543406.2024.2330217
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- Article
The use of real-world data for clinical investigation of effectiveness in drug development.
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- Journal of Biopharmaceutical Statistics, 2024, v. 34, n. 6, p. 818, doi. 10.1080/10543406.2024.2330215
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- Article
On the use of RWD in support of regulatory submission in drug development.
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- Journal of Biopharmaceutical Statistics, 2024, v. 34, n. 6, p. 777, doi. 10.1080/10543406.2024.2330213
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- Article
Analysis of innovative two-stage seamless adaptive design with different endpoints and population shift.
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- Journal of Biopharmaceutical Statistics, 2024, v. 34, n. 6, p. 993, doi. 10.1080/10543406.2024.2330204
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- Article
Unified approaches to assessing treatment effect of traditional Chinese medicine based on health profiles.
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- Journal of Biopharmaceutical Statistics, 2020, v. 30, n. 3, p. 564, doi. 10.1080/10543406.2020.1726368
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- Article
Some thoughts on the QR method for analytical similarity evaluation.
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- Journal of Biopharmaceutical Statistics, 2020, v. 30, n. 3, p. 521, doi. 10.1080/10543406.2020.1726372
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- Article
Innovative design and analysis for rare disease drug development.
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- Journal of Biopharmaceutical Statistics, 2020, v. 30, n. 3, p. 537, doi. 10.1080/10543406.2020.1726371
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- Article
Statistical considerations for rare diseases drug development.
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 874, doi. 10.1080/10543406.2019.1657441
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- Article
Simultaneous confidence interval methods for analytical similarity assessment.
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 920, doi. 10.1080/10543406.2019.1657142
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- Article
The use of 95% CI or 90% CI for drug product development — a controversial issue?
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 834, doi. 10.1080/10543406.2019.1657141
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- Article
Innovative Thinking on Endpoint Selection in Clinical Trials.
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 941, doi. 10.1080/10543406.2019.1657140
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- Article
Probability monitoring procedures for sample size determination.
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 887, doi. 10.1080/10543406.2019.1657139
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- Article
Criteria for dose-finding in two-stage seamless adaptive design.
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 908, doi. 10.1080/10543406.2019.1657130
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- Article
Demonstrating effectiveness or demonstrating not ineffectiveness – A potential solution for rare disease drug product development?
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 5, p. 897, doi. 10.1080/10543406.2019.1657137
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- Article
Interim analysis of binary outcome data in clinical trials: a comparison of five estimators.
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- Journal of Biopharmaceutical Statistics, 2019, v. 29, n. 2, p. 400, doi. 10.1080/10543406.2018.1559852
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- Article
On sample size requirement for analytical similarity assessment.
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- Journal of Biopharmaceutical Statistics, 2018, v. 28, n. 6, p. 1143, doi. 10.1080/10543406.2018.1437171
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- Article
Statistical Methods for Conditional Survival Analysis.
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- Journal of Biopharmaceutical Statistics, 2018, v. 28, n. 5, p. 927, doi. 10.1080/10543406.2017.1405012
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- Article
On evaluation of consistency in multi-regional clinical trials.
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- Journal of Biopharmaceutical Statistics, 2018, v. 28, n. 5, p. 840, doi. 10.1080/10543406.2017.1397008
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- Article
On the evaluation of reliability, repeatability, and reproducibility of instrumental evaluation methods and measurement systems.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 331, doi. 10.1080/10543406.2016.1265547
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- Article
On hybrid parallel–crossover designs for assessing drug interchangeability of biosimilar products.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 265, doi. 10.1080/10543406.2017.1275956
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- Article
Sample size requirement in analytical studies for similarity assessment.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 233, doi. 10.1080/10543406.2016.1265545
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- Article
On safety margin for drug interchangeability.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 293, doi. 10.1080/10543406.2016.1265540
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- Article
On the establishment of equivalence acceptance criterion in analytical similarity assessment.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 206, doi. 10.1080/10543406.2016.1265539
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- Article
Statistical evaluation of the scaled criterion for drug interchangeability.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 282, doi. 10.1080/10543406.2016.1265538
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- Article
Assessing bioequivalence and drug interchangeability.
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- Journal of Biopharmaceutical Statistics, 2017, v. 27, n. 2, p. 272, doi. 10.1080/10543406.2016.1265537
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- Article
On sample size estimation and re-estimation adjusting for variability in confirmatory trials.
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- Journal of Biopharmaceutical Statistics, 2016, v. 26, n. 1, p. 44, doi. 10.1080/10543406.2015.1092031
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- Article
Some thoughts on drug interchangeability.
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- Journal of Biopharmaceutical Statistics, 2016, v. 26, n. 1, p. 178, doi. 10.1080/10543406.2015.1092027
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- Article
On Statistical Tests for Homogeneity of Two Bivariate Zero-Inflated Poisson Populations.
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- Journal of Biopharmaceutical Statistics, 2015, v. 25, n. 1, p. 44, doi. 10.1080/10543406.2014.919934
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- Article
Scientific Factors and Current Issues in Biosimilar Studies.
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- Journal of Biopharmaceutical Statistics, 2014, v. 24, n. 6, p. 1138, doi. 10.1080/10543406.2014.948961
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- Article
Nonparametric Tests for Evaluation of Biosimilarity in Variability of Follow-on Biologics.
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- Journal of Biopharmaceutical Statistics, 2014, v. 24, n. 6, p. 1239, doi. 10.1080/10543406.2014.941991
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- Article
Frequency Estimator for Assessing of Follow-On Biologics.
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- Journal of Biopharmaceutical Statistics, 2014, v. 24, n. 6, p. 1280, doi. 10.1080/10543406.2014.941985
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- Article
Applications of the Bayesian Prior Information to Evaluation of Equivalence of Similar Biological Medicinal Products.
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- Journal of Biopharmaceutical Statistics, 2014, v. 24, n. 6, p. 1254, doi. 10.1080/10543406.2014.941982
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- Article
Sample Size Estimation of Multiregional Clinical Trials with Heterogeneous Variability Across Regions.
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- Journal of Biopharmaceutical Statistics, 2014, v. 24, n. 2, p. 254, doi. 10.1080/10543406.2013.859150
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- Article
Statistical Methods for Bridging Studies.
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- Journal of Biopharmaceutical Statistics, 2012, v. 22, n. 5, p. 903, doi. 10.1080/10543406.2012.701578
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- Publication type:
- Article
Analysis of Time-to-Event Data with Nonuniform Patient Entry and Loss to Follow-Up under a Two-Stage Seamless Adaptive Design with Weibull Distribution.
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- Journal of Biopharmaceutical Statistics, 2012, v. 22, n. 4, p. 773, doi. 10.1080/10543406.2012.678528
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- Article
On the Independence of Data Monitoring Committee in Adaptive Design Clinical Trials.
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- Journal of Biopharmaceutical Statistics, 2012, v. 22, n. 4, p. 853, doi. 10.1080/10543406.2012.676536
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- Article
On Sample Size Calculation for Comparing Survival Curves Under General Hypothesis Testing.
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- Journal of Biopharmaceutical Statistics, 2012, v. 22, n. 3, p. 485, doi. 10.1080/10543406.2010.550701
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- Article
Statistical Inference for Clinical Trials with Binary Responses When There is a Shift in Patient Population.
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- Journal of Biopharmaceutical Statistics, 2011, v. 21, n. 3, p. 437, doi. 10.1080/10543406.2010.481803
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- Article
Imputation Method Adjusted for Covariates for Nonrespondents in Instruments with Applications.
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- Journal of Biopharmaceutical Statistics, 2011, v. 21, n. 2, p. 342, doi. 10.1080/10543406.2011.550114
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- Article