An Adaptive Approach to Implementing Bivariate Group Sequential Clinical Trial Designs

DOI10.1081/BIP-120024197zbMath1197.62153OpenAlexW2001828202WikidataQ47416519 ScholiaQ47416519MaRDI QIDQ4430338

Susan Todd

Publication date: 7 October 2003

Published in: Journal of Biopharmaceutical Statistics (Search for Journal in Brave)

Full work available at URL: https://doi.org/10.1081/bip-120024197

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10) Measures of association (correlation, canonical correlation, etc.) (62H20) Medical applications (general) (92C50) Sequential statistical design (62L05) Sequential statistical analysis (62L10)

Cites Work

• Discrete Sequential Boundaries for Clinical Trials
• Exact Confidence Intervals Following a Group Sequential Test
• Point and interval estimation following a sequential clinical trial
• Group Sequential Tests for Bivariate Response: Interim Analyses of Clinical Trials with Both Efficacy and Safety Endpoints
• Group-Sequential Analysis Incorporating Covariate Information
• Semiparametric Efficiency and Its Implication on the Design and Analysis of Group-Sequential Studies
• Treatment Comparisons Based on Two‐Dimensional Safety and Efficacy Alternatives in Oncology Trials
• Design and analysis of group sequential tests based on the type I error spending rate function
• Evaluation of Experiments with Adaptive Interim Analyses
• Guidelines for Monitoring Efficacy and Toxicity Responses in Clinical Trials
• Nonparametric sequential testing in clinical trials with incomplete multivariate observations

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