DROID: dose-ranging approach to optimizing dose in oncology drug development
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Publication:6589229
DOI10.1111/BIOM.13840zbMATH Open1543.62598MaRDI QIDQ6589229FDOQ6589229
Authors: Beibei Guo, Ying Yuan
Publication date: 19 August 2024
Published in: Biometrics (Search for Journal in Brave)
Cites Work
- Continual Reassessment Method: A Practical Design for Phase 1 Clinical Trials in Cancer
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Title not available (Why is that?)
- Bayesian inference on order-constrained parameters in generalized linear models
- Combining Multiple Comparisons and Modeling Techniques in Dose‐Response Studies
- Bayesian Dose-Finding in Phase I/II Clinical Trials Using Toxicity and Efficacy Odds Ratios
- Bayesian designs for phase I--II clinical trials
- A Bayesian phase I/II trial design for immunotherapy
- Bayesian optimal interval designs for phase I clinical trials
- A utility-based Bayesian optimal interval (U-BOIN) phase I/II design to identify the optimal biological dose for targeted and immune therapies
- gBOIN: a unified model-assisted phase I trial design accounting for toxicity grades, and binary or continuous end points
Cited In (2)
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