Point estimation for adaptive trial designs. I: A methodological review
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Cites work
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Cited in
(14)- A unified Bayesian framework for bias adjustment in multiple comparisons from clinical trials
- Point estimation, confidence intervals, and P-values for optimal adaptive two-stage designs with normal endpoints
- A class of computational methods to reduce selection bias when designing phase 3 clinical trials
- Pitfalls and potentials in simulation studies: questionable research practices in comparative simulation studies allow for spurious claims of superiority of any method
- Point estimation for adaptive trial designs. II: Practical considerations and guidance
- Confidence distributions for treatment effects in clinical trials: posteriors without priors
- Analysis of nonconcurrent controls in adaptive platform trials: separating randomized and nonrandomized information
- Two-stage drop-the-losers design for the selection of effective treatments and estimating their average worth
- Group-sequential designs with an externally-driven change of primary endpoint
- An integrated and coherent framework for point estimation and hypothesis testing with concurrent controls in platform trials
- Adjustment of conditional bias in hazard ratios for group sequential testing of progression-free survival and overall survival
- Statistical inference for a two-stage adaptive seamless design using different binary endpoints
- Statistical Challenges in Online Controlled Experiments: A Review of A/B Testing Methodology
- On the inclusion of non-concurrent controls in platform trials with an interim analysis
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