Bayesian procedures for phase I/II clinical trials investigating the safety and efficacy of drug combinations
Author:
Publisher
Wiley
Subject
Statistics and Probability,Epidemiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/sim.4267/fullpdf
Reference16 articles.
1. A Bayesian dose-finding procedure for phase I clinical trials based only on the assumption of monotonicity;Whitehead;Statistics in Medicine,2010
2. Multiple test procedures for identifying the minimum effective and maximum safe doses of a drug;Tamhane;Journal of the American Statistical Association,2002
3. Identifying effective and/or safe doses by stepwise confidence intervals for ratios;Bretz;Statistics in Medicine,2003
4. A Bayesian dose finding design for dual endpoint phase I trials;Loke;Statistics in Medicine,2006
5. Two-stage design for dose-finding that accounts for both efficacy and safety;Dragalin;Statistics in Medicine,2008
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