Works matching IS 15391604 AND DT 2016 AND VI 15 AND IP 3
Results: 10
Bayesian robustness in meta-analysis for studies with zero responses.
- Published in:
- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 230, doi. 10.1002/pst.1741
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- Article
A win ratio approach to comparing continuous non-normal outcomes in clinical trials.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 238, doi. 10.1002/pst.1743
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- Article
Empirical likelihood based detection procedure for change point in mean residual life functions under random censorship.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 246, doi. 10.1002/pst.1744
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- Article
Decision-making in early clinical drug development.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 255, doi. 10.1002/pst.1746
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- Article
Using Bayesian analysis in repeated preclinical in vivo studies for a more effective use of animals.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 277, doi. 10.1002/pst.1748
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- Article
Modelling PK/QT relationships from Phase I dose-escalation trials for drug combinations and developing quantitative risk assessments of clinically relevant QT prolongations.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 264, doi. 10.1002/pst.1747
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- Article
Predicting analysis time in events-driven clinical trials using accumulating time-to-event surrogate information.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 198, doi. 10.1002/pst.1732
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- Article
Issue Information.
- Published in:
- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 195, doi. 10.1002/pst.1712
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- Article
Distribution of the two-sample t-test statistic following blinded sample size re-estimation.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 208, doi. 10.1002/pst.1737
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- Publication type:
- Article
Sensitivity to censored-at-random assumption in the analysis of time-to-event endpoints.
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- Pharmaceutical Statistics, 2016, v. 15, n. 3, p. 216, doi. 10.1002/pst.1738
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- Article