Sequential Methods in Multi-Arm Clinical Trials
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Publication:3068083
DOI10.1080/07474946.2010.487416zbMath1203.62135OpenAlexW1985549752MaRDI QIDQ3068083
Publication date: 13 January 2011
Published in: Sequential Analysis (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1080/07474946.2010.487416
Applications of statistics to biology and medical sciences; meta analysis (62P10) Bayesian inference (62F15) Medical applications (general) (92C50) Sequential statistical analysis (62L10) Optimal stopping in statistics (62L15)
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Joint task assignment and cache partitioning with cache locking for WCET minimization on MPSoC ⋮ Efficient Adaptive Randomization and Stopping Rules in Multi-arm Clinical Trials for Testing a New Treatment ⋮ Adaptive Dc-optimal designs for dose finding based on a continuous efficacy endpoint
Cites Work
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- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Asymptotic efficiency of three-stage hypothesis tests
- Optimal sequentially planned decision procedures. With the assistance of Günter Duscha, Josef Lübbert and Thomas Meyerthole
- The doubly adaptive biased coin design for sequential clinical trials
- Model-oriented design of experiments
- Bayesian statistics and the efficiency and ethics of clinical trials
- A simple and effective scanning rule for a multi-channel system
- Adaptive designs for selecting drug combinations based on efficacy-toxicity response
- Adaptive designs for dose-finding based on efficacy-toxicity response
- Optimal Designs for Dose-Finding Studies
- On Sample Size and Inference for Two‐Stage Adaptive Designs
- Adaptive Group Sequential Designs for Clinical Trials: Combining the Advantages of Adaptive and of Classical Group Sequential Approaches
- Monitoring Clinical Trials with Multiple Arms
- Dose-Finding Designs for HIV Studies
- Sequential Tests for Noninferiority and Superiority
- Bayesian Optimal Designs for Phase I Clinical Trials
- Discrete Sequential Boundaries for Clinical Trials
- Generalized Likelihood Ratio Statistics and Uncertainty Adjustments in Efficient Adaptive Design of Clinical Trials
- An Application of an Urn Model to the Design of Sequential Controlled Clinical Trials
- Sample size re-estimation without unblinding for normally distributed outcomes with unknown variance
- Designed Extension of Studies Based on Conditional Power
- A Comparison of the Cost‐efficiencies of the Sequential, Group‐sequential, and Variable‐sample‐size‐sequential Probability Ratio Tests
- Recursive Combination Tests
- A Unified Theory of Two-Stage Adaptive Designs
- A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
- Nonparametric Estimation of a Delay Distribution Based on Left‐Censored and Right‐Truncated Data
- Interim Analysis and Sample Size Reassessment
- Monitoring Pairwise Comparisons in Multi-Armed Clinical Trials
- Evaluation of Experiments with Adaptive Interim Analyses
- The Theory of Response‐Adaptive Randomization in Clinical Trials
- A sample size adjustment procedure for clinical trials based on conditional power
- Combining Multiple Comparisons and Modeling Techniques in Dose‐Response Studies
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