Found: 14
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PubPredict: Prediction of progression and survival in oncology leveraging publications and early efficacy data.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 963, doi. 10.1002/pst.2321
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- Article
Determining the minimum duration of treatment in tuberculosis: An order restricted non‐inferiority trial design.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 938, doi. 10.1002/pst.2320
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Defining estimands for efficacy assessment in single arm phase 1b or phase 2 clinical trials in oncology early development.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 921, doi. 10.1002/pst.2319
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- Article
Alone, together: On the benefits of Bayesian borrowing in a meta‐analytic setting.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 903, doi. 10.1002/pst.2318
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Variance estimation of the risk difference when using propensity‐score matching and weighting with time‐to‐event outcomes.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 880, doi. 10.1002/pst.2317
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Replenishing the pipeline: A quantitative approach to optimising the sourcing of new projects.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 861, doi. 10.1002/pst.2316
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Time‐to‐event calibration‐free odds design: A robust efficient design for phase I trials with late‐onset outcomes.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 773, doi. 10.1002/pst.2304
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How to avoid concerns with the interpretation of two primary endpoints if significant superiority in one is sufficient for formal proof of efficacy.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 836, doi. 10.1002/pst.2314
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Bayesian borrowing from historical control data in a vaccine efficacy trial.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 815, doi. 10.1002/pst.2313
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Stability analysis using mixed models: A critique of tolerance interval methods and a probabilistic solution.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 784, doi. 10.1002/pst.2305
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Adaptively leveraging external data with robust meta‐analytical‐predictive prior using empirical Bayes.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 846, doi. 10.1002/pst.2315
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Improved inference for MCP‐Mod approach using time‐to‐event endpoints with small sample sizes.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 760, doi. 10.1002/pst.2303
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- Article
Issue Information.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 757, doi. 10.1002/pst.2239
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- Article
A comparative study of adaptive trial designs for dose optimization.
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- Pharmaceutical Statistics, 2023, v. 22, n. 5, p. 797, doi. 10.1002/pst.2306
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- Article