Sequential methods in multi-arm clinical trials
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Publication:3068083
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Cites work
- scientific article; zbMATH DE number 1332897 (Why is no real title available?)
- scientific article; zbMATH DE number 1348603 (Why is no real title available?)
- scientific article; zbMATH DE number 1369649 (Why is no real title available?)
- A Comparison of the Cost‐efficiencies of the Sequential, Group‐sequential, and Variable‐sample‐size‐sequential Probability Ratio Tests
- A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
- A Unified Theory of Two-Stage Adaptive Designs
- A sample size adjustment procedure for clinical trials based on conditional power
- A simple and effective scanning rule for a multi-channel system
- Adaptive designs for dose-finding based on efficacy-toxicity response
- Adaptive designs for selecting drug combinations based on efficacy-toxicity response
- Adaptive group sequential designs for clinical trials: combining the advantages of adaptive and of classical group sequential approaches
- Adaptive modifications of hypotheses after an interim analysis
- An Application of an Urn Model to the Design of Sequential Controlled Clinical Trials
- Asymptotic efficiency of three-stage hypothesis tests
- Bayesian optimal designs for phase I clinical trials
- Bayesian statistics and the efficiency and ethics of clinical trials
- Combining Multiple Comparisons and Modeling Techniques in Dose‐Response Studies
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Designed Extension of Studies Based on Conditional Power
- Discrete Sequential Boundaries for Clinical Trials
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Dose-finding designs for HIV studies
- Evaluation of Experiments with Adaptive Interim Analyses
- Generalized Likelihood Ratio Statistics and Uncertainty Adjustments in Efficient Adaptive Design of Clinical Trials
- Interim Analysis and Sample Size Reassessment
- Model-oriented design of experiments
- Monitoring Clinical Trials with Multiple Arms
- Monitoring Pairwise Comparisons in Multi-Armed Clinical Trials
- Multiple comparisons of treatments with stable multivariate tests in a two-stage adaptive design, including a test for non-inferiority
- Nonparametric Estimation of a Delay Distribution Based on Left‐Censored and Right‐Truncated Data
- On sample size and inference for two-stage adaptive designs
- Optimal designs for dose-finding studies
- Optimal sequentially planned decision procedures. With the assistance of Günter Duscha, Josef Lübbert and Thomas Meyerthole
- Recursive Combination Tests
- Sample size re-estimation without unblinding for normally distributed outcomes with unknown variance
- Sequential tests for noninferiority and superiority
- The Theory of Response‐Adaptive Randomization in Clinical Trials
- The doubly adaptive biased coin design for sequential clinical trials
Cited in
(10)- Adaptive Dc-optimal designs for dose finding based on a continuous efficacy endpoint
- Impacts on type I error rate with inappropriate use of learn and confirm in confirmatory adaptive design trials
- Sequential monitoring of clinical trials with correlated responses
- Efficient adaptive randomization and stopping rules in multi-arm clinical trials for testing a new treatment
- An O'Brien-Fleming sequential trial for comparing three treatments
- Methodology and application of adaptive and sequential approaches in contemporary clinical trials
- Repeated Randomization and Matching in Multi‐Arm Trials
- Adaptive designs for drug combination informed by longitudinal model for the response
- Joint task assignment and cache partitioning with cache locking for WCET minimization on MPSoC
- Sequential methods for comparative effectiveness experiments: point of care clinical trials
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