Works matching IS 15391604 AND DT 2022 AND VI 21 AND IP 1
Results: 18
A two‐stage drop‐the‐losers design for time‐to‐event outcome using a historical control arm.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 268, doi. 10.1002/pst.2168
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- Article
Methodological challenges in the analysis of recurrent events for randomised controlled trials with application to cardiovascular events in LEADER.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 241, doi. 10.1002/pst.2167
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Flexible diagnostic measures and new cut‐point selection methods under multiple ordered classes.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 220, doi. 10.1002/pst.2166
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- Article
Using an interim analysis based exclusively on an early outcome in a randomized clinical trial with a long‐term clinical endpoint.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 209, doi. 10.1002/pst.2165
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Multiple imputation analysis of Miettinen‐Nurminen interval for difference in proportions.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 196, doi. 10.1002/pst.2162
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Incorporating covariates information in adaptive clinical trials for precision medicine.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 176, doi. 10.1002/pst.2160
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Counterfactual mediation analysis in the multistate model framework for surrogate and clinical time‐to‐event outcomes in randomized controlled trials.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 163, doi. 10.1002/pst.2159
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Estimands for overall survival in clinical trials with treatment switching in oncology.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 150, doi. 10.1002/pst.2158
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Robust estimates of regional treatment effects in multiregional randomized clinical trials with semiparametric logistic model.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 133, doi. 10.1002/pst.2157
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Operational characteristics of generalized pairwise comparisons for hierarchically ordered endpoints.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 122, doi. 10.1002/pst.2156
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Confidence intervals for exposure‐adjusted rate differences in randomized trials.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 103, doi. 10.1002/pst.2155
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Sample size calculation for recurrent event data with additive rates models.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 89, doi. 10.1002/pst.2154
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Flexible parametric copula modeling approaches for clustered survival data.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 69, doi. 10.1002/pst.2153
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- Article
Separation and the information theory surrogate evaluation approach: A penalised likelihood solution.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 55, doi. 10.1002/pst.2152
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- Article
Adjusting for covariates in analysis based on restricted mean survival times.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 38, doi. 10.1002/pst.2151
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- Article
Identifying treatment effect heterogeneity in dose‐finding trials using Bayesian hierarchical models.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 17, doi. 10.1002/pst.2150
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- Article
A unified approach for evaluating the prediction of treatment effect across different types of endpoints.
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- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 4, doi. 10.1002/pst.2149
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- Article
Issue Information.
- Published in:
- Pharmaceutical Statistics, 2022, v. 21, n. 1, p. 1, doi. 10.1002/pst.2133
- Publication type:
- Article