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Use of statistical and pharmacokinetic-pharmacodynamic modeling and simulation to improve decision-making: A section summary report of the trends and innovations in clinical trial statistics conference.
Kimko, Holly; Berry, Seth; O'Kelly, Michael; Mehrotra, Nitin; Hutmacher, Matthew; Sethuraman, Venkat.
Afiliación
  • Kimko H; a Global Clinical Pharmacology , Janssen Research & Development, LLC , Spring House , Pennsylvania , USA.
  • Berry S; b QuintilesIMS, Overland Park , Kansas , USA.
  • O'Kelly M; c QuintilesIMS , Dublin , Ireland.
  • Mehrotra N; d Office of Clinical Pharmacology , Food and Drug Administration , Silver Spring , Maryland , USA.
  • Hutmacher M; e Ann Arbor Pharmacometrics Group , Ann Arbor , Michigan , USA.
  • Sethuraman V; f Bristol-Myers Squibb, LLC , Princeton , New Jersey , USA.
J Biopharm Stat ; 27(3): 554-567, 2017.
Article en En | MEDLINE | ID: mdl-28304215
ABSTRACT
The application of modeling and simulation (M&S) methods to improve decision-making was discussed during the Trends & Innovations in Clinical Trial Statistics Conference held in Durham, North Carolina, USA on May 1-4, 2016. Uses of both pharmacometric and statistical M&S were presented during the conference, highlighting the diversity of the methods employed by pharmacometricians and statisticians to address a broad range of quantitative issues in drug development. Five presentations are summarized herein, which cover the development strategy of employing M&S to drive decision-making; European initiatives on best practice in M&S; case studies of pharmacokinetic/pharmacodynamics modeling in regulatory decisions; estimation of exposure-response relationships in the presence of confounding; and the utility of estimating the probability of a correct decision for dose selection when prior information is limited. While M&S has been widely used during the last few decades, it is expected to play an essential role as more quantitative assessments are employed in the decision-making process. By integrating M&S as a tool to compile the totality of evidence collected throughout the drug development program, more informed decisions will be made.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Simulación por Computador / Farmacocinética / Modelos Estadísticos / Toma de Decisiones Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Simulación por Computador / Farmacocinética / Modelos Estadísticos / Toma de Decisiones Tipo de estudio: Guideline / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2017 Tipo del documento: Article