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Bayesian Methods in Human Drug and Biological Products Development in CDER and CBER

The Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) of the U.S. Food and Drug Administration (FDA) have been leaders in protecting and promoting the U.S. public health by helping to ensure that safe and effective drugs and biological product...

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Detalles Bibliográficos
Autores principales: Ionan, Alexei C., Clark, Jennifer, Travis, James, Amatya, Anup, Scott, John, Smith, James P., Chattopadhyay, Somesh, Salerno, Mary Jo, Rothmann, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9718464/
https://www.ncbi.nlm.nih.gov/pubmed/36459346
http://dx.doi.org/10.1007/s43441-022-00483-0
Descripción
Sumario:The Center for Drug Evaluation and Research (CDER) and the Center for Biologics Evaluation and Research (CBER) of the U.S. Food and Drug Administration (FDA) have been leaders in protecting and promoting the U.S. public health by helping to ensure that safe and effective drugs and biological products are available in the United States for those who need them. The null hypothesis significance testing approach, along with other considerations, is typically used to demonstrate the effectiveness of a drug or biological product. The Bayesian framework presents an alternative approach to demonstrate the effectiveness of a treatment. This article discusses the Bayesian framework for drug and biological product development, highlights key settings in which Bayesian approaches may be appropriate, and provides recent examples of the use of Bayesian approaches within CDER and CBER.