Bayesian optimization design for finding a maximum tolerated dose combination in phase I clinical trials
From MaRDI portal
Publication:6637076
DOI10.1515/IJB-2020-0147MaRDI QIDQ6637076
Publication date: 13 November 2024
Published in: The International Journal of Biostatistics (Search for Journal in Brave)
maximum tolerated dosecombination therapynonparametric methodBayesian optimizationphase I clinical trials
Cites Work
- Title not available (Why is that?)
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Dose finding with escalation with overdose control (EWOC) in cancer clinical trials
- Efficient global optimization of expensive black-box functions
- Continual Reassessment Method for Partial Ordering
- Cancer phase I trial design using drug combinations when a fraction of dose limiting toxicities is attributable to one or more agents
- Convergence rates of efficient global optimization algorithms
- Two‐Dimensional Dose Finding in Discrete Dose Space
- Bayesian optimal interval designs for phase I clinical trials
This page was built for publication: Bayesian optimization design for finding a maximum tolerated dose combination in phase I clinical trials
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q6637076)