A Bayesian phase I/II trial design for immunotherapy
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Publication:4559685
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- scientific article; zbMATH DE number 2242805
- A Parallel Phase I/II Clinical Trial Design for Combination Therapies
Cites work
- scientific article; zbMATH DE number 2117879 (Why is no real title available?)
- Bayesian Dose-Finding in Phase I/II Clinical Trials Using Toxicity and Efficacy Odds Ratios
- Bayesian designs for phase I--II clinical trials
- Bayesian phase I/II adaptively randomized oncology trials with combined drugs
- Dose-Finding Based on Efficacy-Toxicity Trade-Offs
- Using joint utilities of the times to response and toxicity to adaptively optimize schedule-dose regimes
- Utility-Based Optimization of Combination Therapy Using Ordinal Toxicity and Efficacy in Phase I/II Trials
Cited in
(9)- A Bayesian adaptive design for dual-agent phase I-II oncology trials integrating efficacy data across stages
- Biomarker-based precision dose finding for immunotherapy combined with radiotherapy
- BIPSE: a biomarker-based phase I/II design for immunotherapy trials with progression-free survival endpoint
- DROID: dose-ranging approach to optimizing dose in oncology drug development
- A Bayesian design for phase I cancer therapeutic vaccine trials
- REDOMA: Bayesian random-effects dose-optimization meta-analysis using spike-and-slab priors
- A Bayesian phase I/II platform design for co-developing drug combination therapies for multiple indications
- Hybrid design evaluating new biomarkers when there is an existing screening test
- A Bayesian adaptive phase i/II platform trial design for pediatric immunotherapy trials
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