Specifications of a continual reassessment method design for phase I trials of combined drugs-Reference-Cited by-同舟云学术

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Specifications of a continual reassessment method design for phase I trials of combined drugs

Published:2013-06-03 Issue:4 Volume:12 Page:217-224
ISSN:1539-1604
Container-title:Pharmaceutical Statistics
language:en
Short-container-title:Pharmaceut. Statist.

Author:

Wages Nolan A.¹,Conaway Mark R.¹

Affiliation:

1. Division of Translational Research and Applied Statistics, Department of Public Health Sciences; University of Virginia; Charlottesville VA USA

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pst.1575/fullpdf

Reference17 articles.

1. Continual reassessment method for partial ordering;Wages;Biometrics,2011a

2. Continual reassessment method: a practical design for phase I clinical trials in cancer;O'Quigley;Biometrics,1990

3. Designs for single-or multiple-agent phase I trials;Conaway;Biometrics,2004

4. Bayesian dose finding for drug combinations by copula regression;Yin;Journal of the Royal Statistical Society,2009a

5. A latent contingency table approach to dose-finding for combinations of two agents;Yin;Biometrics,2009b

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