TWO-SAMPLE CONTINUAL REASSESSMENT METHOD
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Publication:4244513
DOI10.1081/BIP-100100998zbMATH Open0919.62123OpenAlexW1991092971WikidataQ41616151 ScholiaQ41616151MaRDI QIDQ4244513FDOQ4244513
Authors: John O'Quigley, Larry Zaiqian Shen, A. C. Gamst 
Publication date: 5 September 1999
Published in: Journal of Biopharmaceutical Statistics (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1081/bip-100100998
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Applications of statistics to biology and medical sciences; meta analysis (62P10) Sequential statistical design (62L05)
Cited In (14)
- Individualized dosing for multiple ordered groups of patients
- Patient-specific dose finding in phase I clinical trials
- Incorporating a patient dichotomous characteristic in cancer phase I clinical trials using escalation with overdose control
- Continual reassessment method for ordered groups
- Dose finding with escalation with overdose control (EWOC) in cancer clinical trials
- Bayesian adaptive design of early-phase clinical trials for precision medicine based on cancer biomarkers
- Theoretical study of the continual reassessment method
- Adaptive clinical trial designs for phase I cancer studies
- Efficiency of bridging between related dose finding studies
- The Continual Reassessment Method for Multiple Toxicity Grades: A Bayesian Quasi‐Likelihood Approach
- Continual reassessment and related dose-finding designs
- Design efficiency in dose finding studies
- A Bayesian adaptive design in cancer phase I trials using dose combinations in the presence of a baseline covariate
- Patient‐Specific Dose Finding Based on Bivariate Outcomes and Covariates
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