An Adaptive Approach to Implementing Bivariate Group Sequential Clinical Trial Designs

DOI10.1081/BIP-120024197MaRDI QIDQ4430338zbMATH OpenOpenAlexWikidataFDO

Authors 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

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

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Cites work

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

Cited in

(7)

• Methodology and application of adaptive and sequential approaches in contemporary clinical trials
• Group-sequential logrank methods for trial designs using bivariate non-competing event-time outcomes
• scientific article; zbMATH DE number 2015226 (Why is no real title available?)
• Planning and Analyzing Adaptive Group Sequential Survival Trials
• scientific article; zbMATH DE number 5032141 (Why is no real title available?)
• Adaptive Design and Estimation in Randomized Clinical Trials with Correlated Observations
• Group sequential designs for clinical trials with bivariate endpoints

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