Optimal designs for contingent response models with application to toxicity-efficacy studies
DOI10.1016/J.JSPI.2013.03.025zbMATH Open1278.62117OpenAlexW2069728914MaRDI QIDQ389259FDOQ389259
Authors: Huwaida Rabie, Nancy Flournoy
Publication date: 20 January 2014
Published in: Journal of Statistical Planning and Inference (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1016/j.jspi.2013.03.025
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dose-findingbivariate responsescontinuation ratio modelexperimental designsnonlinear response functionsphase II clinical trials
Applications of statistics to biology and medical sciences; meta analysis (62P10) Optimal statistical designs (62K05)
Cites Work
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- Penalized optimal designs for dose-finding
- Optimal designs and limiting optimal designs for a trinomial response
- Compound optimal allocation for individual and collective ethics in binary clinical trials
- Some Properties for a Simplified Cox Binary Model
- Optimal designs for contingent response models with application to toxicity-efficacy studies
- A sequential design for maximizing the probability of a favourable response
- Approximate dynamic programming and its applications to the design of Phase I cancer trials
Cited In (12)
- Optimal designs for discriminating between dose-response models in toxicology studies
- On optimal designs for clinical trials: an updated review
- Optimal adaptive designs for acute oral toxicity assessment
- Optimal designs and limiting optimal designs for a trinomial response
- Optimal designs for response functions with a downturn
- A response-driven adaptive design based on the Klein urn
- Optimal experimental designs for estimating the drug combination index in toxicology
- Optimal designs for dose-finding experiments in toxicity studies
- Optimal cutpoints for random observations
- Optimal design to discriminate between rival copula models for a bivariate binary response
- Optimal designs for contingent response models with application to toxicity-efficacy studies
- Optimal designs for estimating critical effective dose under model uncertainty in a dose response study
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