DICE: A Bayesian model for early dose finding in phase I trials with multiple treatment courses
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Publication:6068878
DOI10.1002/bimj.202000369zbMath1523.62223OpenAlexW3208368031MaRDI QIDQ6068878
Moreno Ursino, Unnamed Author, Sylvie Chevret
Publication date: 15 December 2023
Published in: Biometrical Journal (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1002/bimj.202000369
Cites Work
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- A Phase I Bayesian Adaptive Design to Simultaneously Optimize Dose and Schedule Assignments Both Between and Within Patients
- Determining the Effective Sample Size of a Parametric Prior
- Sequential Designs for Phase I Clinical Trials with Late‐Onset Toxicities
- Determining a Maximum‐Tolerated Schedule of a Cytotoxic Agent
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