Works matching IS 15391604 AND DT 2024 AND VI 23 AND IP 6
Results: 28
Applying the Estimand Framework to Non‐Inferiority Trials.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1156, doi. 10.1002/pst.2433
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Bayesian Methods for Quality Tolerance Limit (QTL) Monitoring.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1166, doi. 10.1002/pst.2427
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Efficient Study Design and Analysis of Longitudinal Dose–Response Data Using Fractional Polynomials.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1128, doi. 10.1002/pst.2425
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Bayesian Hierarchical Models for Subgroup Analysis.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1065, doi. 10.1002/pst.2424
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Reparametrized Firth's Logistic Regressions for Dose‐Finding Study With the Biased‐Coin Design.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1117, doi. 10.1002/pst.2423
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- Article
Exploring Stratification Strategies for Population‐ Versus Randomization‐Based Inference.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1045, doi. 10.1002/pst.2419
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Variable Duration Trial as an Alternative Design for Continuous Endpoints.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1059, doi. 10.1002/pst.2418
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A Personalized Dose‐Finding Algorithm Based on Adaptive Gaussian Process Regression.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1181, doi. 10.1002/pst.2417
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Handling Partially Observed Trial Data After Treatment Withdrawal: Introducing Retrieved Dropout Reference‐Base Centred Multiple Imputation.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1095, doi. 10.1002/pst.2416
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- Article
Survival Analysis Without Sharing of Individual Patient Data by Using a Gaussian Copula.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1031, doi. 10.1002/pst.2415
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- Article
T3 + 3: 3 + 3 Design With Delayed Outcomes.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 959, doi. 10.1002/pst.2414
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- Article
Optimal Cut‐Point Selection Methods Under Binary Classification When Subclasses Are Involved.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 984, doi. 10.1002/pst.2413
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Do You Want to Stay Single? Considerations on Single‐Arm Trials in Drug Development and the Postregulatory Space.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1206, doi. 10.1002/pst.2412
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- Article
Estimation of Treatment Policy Estimands for Continuous Outcomes Using Off‐Treatment Sequential Multiple Imputation.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1144, doi. 10.1002/pst.2411
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- Article
Futility Interim Analysis Based on Probability of Success Using a Surrogate Endpoint.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 971, doi. 10.1002/pst.2410
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- Article
Investigating Stability in Subgroup Identification for Stratified Medicine.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 945, doi. 10.1002/pst.2409
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- Article
Sample Size Estimation Using a Partially Clustered Frailty Model for Biomarker‐Strategy Designs With Multiple Treatments.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 1084, doi. 10.1002/pst.2407
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- Article
To Dilute or Not to Dilute: Nominal Titer Dosing for Genetic Medicines.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 939, doi. 10.1002/pst.2406
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- Article
Using an early outcome as the sole source of information of interim decisions regarding treatment effect on a long‐term endpoint: The non‐Gaussian case.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 928, doi. 10.1002/pst.2398
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- Article
Covariate adjustment and estimation of difference in proportions in randomized clinical trials.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 884, doi. 10.1002/pst.2397
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A model‐assisted design for partially or completely ordered groups.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 906, doi. 10.1002/pst.2396
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Current developments of the estimand concept.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 864, doi. 10.1002/pst.2395
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Optimal sample size division in two‐stage seamless designs.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 854, doi. 10.1002/pst.2394
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Visualizing hypothesis tests in survival analysis under anticipated delayed effects.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 870, doi. 10.1002/pst.2393
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Comparing various Bayesian random‐effects models for pooling randomized controlled trials with rare events.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 837, doi. 10.1002/pst.2392
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Tree‐temporal scan statistics for safety signal detection in vaccine clinical trials.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 813, doi. 10.1002/pst.2391
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Mathematical programming tools for randomization purposes in small two‐arm clinical trials: A case study with real data.
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- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 794, doi. 10.1002/pst.2388
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Issue Information.
- Published in:
- Pharmaceutical Statistics, 2024, v. 23, n. 6, p. 791, doi. 10.1002/pst.2312
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- Article