Precision generalized phase I--II designs
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Cites work
- A Strategy for Dose-Finding and Safety Monitoring Based on Efficacy and Adverse Outcomes in Phase I/II Clinical Trials
- Analysis of multivariate probit models
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Phase I/II design for selecting subgroup-specific optimal biological doses for prespecified subgroups
- Precision Bayesian phase I-II dose-finding based on utilities tailored to prognostic subgroups
- Reversible jump Markov chain Monte Carlo computation and Bayesian model determination
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