Point estimation for adaptive trial designs. I: A methodological review
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Publication:6629916
DOI10.1002/SIM.9605zbMATH Open1548.6241MaRDI QIDQ6629916
Philip Pallmann, David S. Robertson, Babak Choodari-Oskooei, Laura Flight, Thomas Jaki, Munya Dimairo
Publication date: 30 October 2024
Published in: Statistics in Medicine (Search for Journal in Brave)
Cites Work
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- Completeness and unbiased estimation of mean vector in the multivariate group sequential case
- On Bayesian estimators in multistage binomial designs
- Two stage conditionally unbiased estimators of the selected mean
- Sequential estimation for two-stage and three-stage clinical trials
- Bootstrap corrections of treatment effect estimates following selection
- An efficient sequential design of clinical trials
- A general framework for the analysis of adaptive experiments
- Estimation following selection of the largest of two normal means
- On design and inference for two-stage adaptive clinical trials with dependent data
- Point estimates and confidence regions for sequential trials involving selection
- Unbiased estimation of secondary parameters following a sequential test
- Conditional point estimation in adaptive group sequential test designs
- Inference about a secondary process following a sequential trial
- Group Sequential and Confirmatory Adaptive Designs in Clinical Trials
- Simultaneous confidence intervals that are compatible with closed testing in adaptive designs
- A generalized Dunnett test for multi-arm multi-stage clinical studies with treatment selection
- An evaluation of inferential procedures for adaptive clinical trial designs with pre-specified rules for modifying the sample size
- Likelihood inference for a two-stage design with treatment selection
- Parameter estimation following an adaptive treatment selection trial design
- On Sample Size and Inference for Two‐Stage Adaptive Designs
- Estimation of a Secondary Parameter in a Group Sequential Clinical Trial
- Adaptive Group Sequential Designs for Clinical Trials: Combining the Advantages of Adaptive and of Classical Group Sequential Approaches
- Test-compatible confidence intervals for adaptive two-stage single-arm designs with binary endpoint
- Unbiased estimation of the parameter of a selected binomial population
- Point Estimation Following Group Sequential Tests
- Estimation of a Parameter and Its Exact Confidence Interval Following Sequential Sample Size Reestimation Trials
- Adaptive design: estimation and inference with censored data in a semiparametric model
- Exact Confidence Bounds Following Adaptive Group Sequential Tests
- Improved approximation for estimation following closed sequential tests
- Point and interval estimation following a sequential clinical trial
- Estimation after sequential testing: A simple approach for a truncated sequential probability ratio test
- Unbiased estimation following a group sequential test
- Bias Reduction using Stochastic Approximation
- Conditional estimation following a group sequential clinical trial
- A Computationally Simpler Algorithm for the UMVUE of a Normal Mean Following a Group Sequential Trial
- Bias reduction via resampling for estimation following sequential tests
- Estimating and reducing bias in group sequential designs with Gaussian independent increment structure
- Sequential tests and estimators after overrunning based on maximum-likelihood ordering
- Recursive Combination Tests
- Sample Size Reestimation for Clinical Trials With Censored Survival Data
- A Unified Theory of Two-Stage Adaptive Designs
- ESTIMATION FOLLOWING EXTENSION OF A STUDY ON THE BASIS OF CONDITIONAL POWER
- Statistical Inference for Self‐Designing Clinical Trials with a One‐Sided Hypothesis
- Adaptive Sample Size Calculations in Group Sequential Trials
- On the bias of maximum likelihood estimation following a sequential test
- Supplementary Analysis at the Conclusion of a Sequential Clinical Trial
- Evaluation of Experiments with Adaptive Interim Analyses
- Confidence intervals for confirmatory adaptive two‐stage designs with treatment selection
- Adaptive designs for noninferiority trials
- Conditionally unbiased estimation in the normal setting with unknown variances
- Estimation and Confidence Intervals after Adjusting the Maximum Information
- Sample Size Reassessment in Adaptive Clinical Trials Using a Bias Corrected Estimate
- Conditional Maximum Likelihood Estimation Following a Group Sequential Test
- Planning and Analyzing Adaptive Group Sequential Survival Trials
- Unbiased Estimation of Selected Treatment Means in Two‐Stage Trials
- Familywise error control in multi‐armed response‐adaptive trials
- Uniformly minimum variance conditionally unbiased estimation in multi-arm multi-stage clinical trials
- Conditionally unbiased and near unbiased estimation of the selected treatment mean for multistage drop‐the‐losers trials
- Conditional Estimation in Two-Stage Adaptive Designs
- Estimation of treatment effects following a sequential trial of multiple treatments
- Estimation of treatment effect in 2-in-1 adaptive design and some of its extensions
- A comparison of estimation methods adjusting for selection bias in adaptive enrichment designs with time-to-event endpoints
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