Abstract
Most methods for sequentially adaptive dose-finding in phase I clinical trials characterize outcome as an indicator yt of toxicity and assume that patients are homogeneous. This entry reviews a new method which requires an informative prior on covariate effect parameters, obtained from historical data.
| Original language | English (US) |
|---|---|
| Title of host publication | Encyclopedia of Biopharmaceutical Statistics - Four Volume Set |
| Publisher | CRC Press |
| Pages | 760-771 |
| Number of pages | 12 |
| Volume | 1-4 |
| ISBN (Electronic) | 9781351110266 |
| ISBN (Print) | 9781351110259 |
| DOIs | |
| State | Published - Jan 1 2018 |
Keywords
- Adaptive design
- Bayesian design
- Individualized treatment
- Phase I clinical trial
- Phase I/II clinical trial.
ASJC Scopus subject areas
- General Medicine
- General Mathematics
- General Biochemistry, Genetics and Molecular Biology
- General Agricultural and Biological Sciences
- General Pharmacology, Toxicology and Pharmaceutics
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