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An optimised multi-arm multi-stage clinical trial design for unknown variance

Multi-arm multi-stage trial designs can bring notable gains in efficiency to the drug development process. However, for normally distributed endpoints, the determination of a design typically depends on the assumption that the patient variance in response is known. In practice, this will not usually...

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Dades bibliogràfiques
Publicat a:Contemp Clin Trials
Autors principals: Grayling, Michael J., Wason, James M.S., Mander, Adrian P.
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5886309/
https://ncbi.nlm.nih.gov/pubmed/29474933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cct.2018.02.011
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