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Bayesian Methods in Human Drug and Biological Products Development in CDER and CBER.
Ionan, Alexei C; Clark, Jennifer; Travis, James; Amatya, Anup; Scott, John; Smith, James P; Chattopadhyay, Somesh; Salerno, Mary Jo; Rothmann, Mark.
  • Ionan AC; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA. Alexei.Ionan@fda.hhs.gov.
  • Clark J; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Travis J; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Amatya A; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Scott J; Division of Biostatistics, Center for Biologics Evaluation and Research, Office of Biostatistics and Pharmacovigilance, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Smith JP; Center for Drug Evaluation and Research, Office of New Drugs, Office of New Drug Policy, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Chattopadhyay S; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Salerno MJ; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA.
  • Rothmann M; Center for Drug Evaluation and Research, Office of Translational Sciences, Office of Biostatistics, U.S. Food and Drug Administration, Silver Spring, MD, USA.
Ther Innov Regul Sci ; 2022 Dec 02.
Article in English | MEDLINE | ID: covidwho-2323759
ABSTRACT
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.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Language: English Year: 2022 Document Type: Article Affiliation country: S43441-022-00483-0

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Experimental Studies Language: English Year: 2022 Document Type: Article Affiliation country: S43441-022-00483-0