A Versatile Adaptive Dose-Finding Design Based on Multiple Endpoints
Author:
Affiliation:
1. Capionis, Bordeaux, France
2. Biometrics Division, H. Lundbeck A/S, Valby, Denmark
3. Department of Biostatistics, University of Copenhagen, Copenhagen, Denmark
Publisher
Informa UK Limited
Subject
Pharmaceutical Science,Statistics and Probability
Link
https://www.tandfonline.com/doi/pdf/10.1080/19466315.2017.1341333
Reference29 articles.
1. A Bayesian Approach to Jointly Modeling Toxicity and Biomarker Expression in a Phase I/II Dose-Finding Trial
2. Bornkamp, B., Pinheiro, J., and Bretz, F. (2014), “Dosefinding: Planning and c, 2014,” R Package Version 0.9-5, available at http://CRAN.R-project.org/package=DoseFinding.
3. The bivariate continual reassessment method
4. Designing Experiments with Respect to 'Standardized' Optimality Criteria
5. Innovation in the pharmaceutical industry: New estimates of R&D costs
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2. Key Aspects of Modern, Quantitative Drug Development;Statistics in Biosciences;2018-05-10
3. Assessing the similarity of dose response and target doses in two non-overlapping subgroups;Statistics in Medicine;2017-11-27
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