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Time-to-event Bayesian Optimal Interval Design to Accelerate Phase I Trials

Late-onset toxicity is common for novel molecularly targeted agents and immunotherapy. It causes major logistic difficulty for existing adaptive phase I trial designs, which require the observance of toxicity early enough to apply dose escalation rules for new patients. The same logistic difficulty...

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Detalhes bibliográficos
Publicado no:Clin Cancer Res
Main Authors: Yuan, Ying, Lin, Ruitao, Li, Daniel, Nie, Lei, Warren, Katherine E.
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6191365/
https://ncbi.nlm.nih.gov/pubmed/29769209
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/1078-0432.CCR-18-0246
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