A trivariate continual reassessment method for phase I/II trials of toxicity, efficacy, and surrogate efficacy
Author:
Affiliation:
1. Division of Biostatistics; University of Minnesota; U.S.A.
Funder
NCI
Publisher
Wiley
Subject
Statistics and Probability,Epidemiology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/sim.5477/fullpdf
Reference19 articles.
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3. Bayesian Adaptive Methods for Clinical Trials
4. Pharmacologically guided phase I clinical trials based upon preclinical drug development;Collins;Journal of the National Cancer Institute,1990
5. Design and analysis of phase I clinical trials;Storer;Biometrics,1989
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