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On the Use of Local Assessments for Monitoring Centrally Reviewed Endpoints with Missing Data in Clinical Trials()

Due to ethical and logistical concerns it is common for data monitoring committees to periodically monitor accruing clinical trial data to assess the safety, and possibly efficacy, of a new experimental treatment. When formalized, monitoring is typically implemented using group sequential methods. I...

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Detalles Bibliográficos
Autores principales: Brummel, Sean S., Gillen, Daniel L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273501/
https://www.ncbi.nlm.nih.gov/pubmed/25540717
http://dx.doi.org/10.4236/ojs.2013.34A005