Works matching IS 15391604 AND DT 2014 AND VI 13 AND IP 4
Results: 9
Subgroup analyses in cost-effectiveness analyses to support health technology assessments.
- Published in:
- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 265, doi. 10.1002/pst.1626
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- Article
Missing data sensitivity analysis for recurrent event data using controlled imputation.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 258, doi. 10.1002/pst.1624
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- Article
Drug development: EU paediatric legislation, the European Medicines Agency and its Paediatric Committee-adolescents' melanoma as a paradigm.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 211, doi. 10.1002/pst.1623
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- Article
When is a seamless study desirable? Case studies from different pharmaceutical sponsors.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 229, doi. 10.1002/pst.1622
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- Article
Benefit-risk assessment in pharmaceutical research and development.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 275, doi. 10.1002/pst.1627
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- Article
Data-driven treatment selection for seamless phase II/III trials incorporating early-outcome data.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 238, doi. 10.1002/pst.1619
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- Article
A Bayesian dose-finding design for drug combination clinical trials based on the logistic model.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 247, doi. 10.1002/pst.1621
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- Article
Statistical considerations associated with a comprehensive regulatory framework to address the unmet need for new antibacterial therapies.
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 222, doi. 10.1002/pst.1625
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- Article
Can a treatment be licenced on the basis of post-treatment predictive biomarkers?
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- Pharmaceutical Statistics, 2014, v. 13, n. 4, p. 214, doi. 10.1002/pst.1620
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- Article