A study design with conditional, serially assessed co-primary endpoints: An application to a single-arm, pilot non-Hodgkin's lymphoma trial-Reference-Cited by-同舟云学术

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A study design with conditional, serially assessed co-primary endpoints: An application to a single-arm, pilot non-Hodgkin's lymphoma trial

Published:2010-10-15 Issue:7 Volume:71 Page:395-403
ISSN:0272-4391
Container-title:Drug Development Research
language:en
Short-container-title:Drug Dev. Res.

Author:

Mahnken Jonathan D.,Wick Jo A.,Gajewski Byron J.,Mayo Matthew S.

Publisher

Wiley

Subject

Drug Discovery

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ddr.20387/fullpdf

Reference27 articles.

1. Categorical Data Analysis

2. Incorporating toxicity considerations into the design of two-stage phase ii clinical trials;Bryant;Biometrics,1995

3. Bivariate sequential designs for phase II trial;Conaway;Biometrics,1995

4. Designs for phase ii trials allowing for a trade-off between response and toxicity;Conaway;Biometrics,1996

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