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The Randomized CRM: An Approach to Overcoming the Long-Memory Property of the CRM

The primary object of a phase I clinical trial is to determine the maximum tolerated dose (MTD). Typically, the MTD is identified using a dose-escalation study, where initial subjects are treated at the lowest dose level and subsequent subjects are treated at progressively higher dose levels until t...

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Detalhes bibliográficos
Publicado no:J Biopharm Stat
Main Authors: Koopmeiners, Joseph S., Wey, Andrew
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5581285/
https://ncbi.nlm.nih.gov/pubmed/28340333
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/10543406.2017.1293076
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