Incorporating patient-reported outcomes in dose-finding clinical trials with continuous patient enrollment

Andrillon, A., Biard, L., & Lee, S. M. (2023). Incorporating patient-reported outcomes in dose-finding clinical trials with continuous patient enrollment. Journal of Biopharmaceutical Statistics, 1–12. https://doi.org/10.1080/10543406.2023.2236216
Authors:
Anaïs Andrillon
Lucie Biard
Shing M Lee
Affiliated Authors:
Shing M Lee
Columbia Affiliation:
Author Keywords:
accelerated dose finding
bayesian adaptive dose finding
continual reassessment method
late-onset toxicities
multiple toxicity constraints
partial toxicity follow-up
phase i trial
time-to-event
elink
Publication Type:
Article
Unique ID:
10.1080/10543406.2023.2236216
PMID:
37496233
DOI:
10.1080/10543406.2023.2236216
Journal:
Journal of Biopharmaceutical Statistics
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record

Record Created: