Works matching IS 15391604 AND DT 2021 AND VI 20 AND IP 4
Results: 16
Search for relevant subsets of binary predictors in high dimensional regression for discovering the lead molecule.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 898, doi. 10.1002/pst.2117
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A simulation‐free group sequential design with max‐combo tests in the presence of non‐proportional hazards.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 879, doi. 10.1002/pst.2116
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- Article
Progression‐free survival in oncological clinical studies: Assessment time bias and methods for its correction.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 864, doi. 10.1002/pst.2115
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Logistic retainment interval dose exploration design for Phase I clinical trials of cytotoxic agents.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 850, doi. 10.1002/pst.2114
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Using recurrent time‐to‐event models with multinomial outcomes to generate toxicity profiles.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 840, doi. 10.1002/pst.2113
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Power and sample size for GEE analysis of incomplete paired outcomes in 2 × 2 crossover trials.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 820, doi. 10.1002/pst.2112
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Matrix decomposition in meta‐analysis for extraction of adverse event pattern and patient‐level safety profile.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 806, doi. 10.1002/pst.2109
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- Article
Estimands in hematologic oncology trials.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 793, doi. 10.1002/pst.2108
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- Article
How to choose a time zero for patients in external control arms.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 783, doi. 10.1002/pst.2107
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A comparison of reweighting estimators of average treatment effects in real world populations.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 765, doi. 10.1002/pst.2106
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On kernel machine learning for propensity score estimation under complex confounding structures.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 752, doi. 10.1002/pst.2105
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- Article
Principal stratum strategy: Potential role in drug development.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 737, doi. 10.1002/pst.2104
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Statistical considerations in clinical trial design with event‐free survival as the primary efficacy endpoint.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 721, doi. 10.1002/pst.2103
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- Article
Optimising the trade‐off between type I and II error rates in the Bayesian context.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 710, doi. 10.1002/pst.2102
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- Article
A robust permutation test for the concordance correlation coefficient.
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- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 696, doi. 10.1002/pst.2101
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- Article
Issue Information.
- Published in:
- Pharmaceutical Statistics, 2021, v. 20, n. 4, p. 693, doi. 10.1002/pst.2036
- Publication type:
- Article