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Pediatric Pharmacokinetics and Dose Predictions: A Report of a Satellite Meeting to the 10th Juvenile Toxicity Symposium.
van Groen, Bianca D; Pilla Reddy, Venkatesh; Badée, Justine; Olivares-Morales, Andrés; Johnson, Trevor N; Nicolaï, Johan; Annaert, Pieter; Smits, Anne; de Wildt, Saskia N; Knibbe, Catherijne A J; de Zwart, Loeckie.
Afiliação
  • van Groen BD; Intensive Care and Department of Pediatric Surgery, Erasmus MC-Sophia Children's Hospital, Rotterdam, The Netherlands.
  • Pilla Reddy V; Roche Pharma and Early Development (pRED), Roche Innovation Center Basel, Basel, Switzerland.
  • Badée J; Modelling and Simulation, Early Oncology, Oncology R&D, AstraZeneca, Cambridge, UK.
  • Olivares-Morales A; Center for Pharmacometrics & Systems Pharmacology, Department of Pharmaceutics, University of Florida at Lake Nona, Orlando, Florida, USA.
  • Johnson TN; Modelling & Simulation, Novartis Institutes for Biomedical Research, Basel, Switzerland.
  • Nicolaï J; Roche Pharma and Early Development (pRED), Roche Innovation Center Basel, Basel, Switzerland.
  • Annaert P; Certara UK Limited (Simcyp), Sheffield, UK.
  • Smits A; Development Science, UCB BioPharma SRL, Braine-l'Alleud, Belgium.
  • de Wildt SN; Drug Delivery and Disposition, KU Leuven Department of Pharmaceutical and Pharmacological Sciences, Leuven, Belgium.
  • Knibbe CAJ; Neonatal Intensive Care Unit, University Hospitals Leuven, Leuven, Belgium.
  • de Zwart L; Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Clin Transl Sci ; 14(1): 29-35, 2021 01.
Article em En | MEDLINE | ID: mdl-32702198
On April 24, 2019, a symposium on Pediatric Pharmacokinetics and Dose Predictions was held as a satellite meeting to the 10th Juvenile Toxicity Symposium. This symposium brought together scientists from academia, industry, and clinical research organizations with the aim to update each other on the current knowledge on pediatric drug development. Through more knowledge on specific ontogeny profiles of drug metabolism and transporter proteins, integrated into physiologically-based pharmacokinetic (PBPK) models, we have gained a more integrated understanding of age-related differences in pharmacokinetics (PKs), Relevant examples were presented during the meeting. PBPK may be considered the gold standard for pediatric PK prediction, but still it is important to know that simpler methods, such as allometry, allometry combined with maturation function, functions based on the elimination pathway, or linear models, also perform well, depending on the age range or the mechanisms involved. Knowledge from different methods and information sources should be combined (e.g., microdosing can reveal early read-out of age-related differences in exposure), and such results can be a value to verify models. To further establish best practices for dose setting in pediatrics, more in vitro and in vivo research is needed on aspects such as age-related changes in the exposure-response relationship and the impact of disease on PK. New information coupled with the refining of model-based drug development approaches will allow faster targeting of intended age groups and allow more efficient design of pediatric clinical trials.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Taxa de Depuração Metabólica / Relação Dose-Resposta a Droga / Modelos Biológicos Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Taxa de Depuração Metabólica / Relação Dose-Resposta a Droga / Modelos Biológicos Tipo de estudo: Guideline / Prognostic_studies / Risk_factors_studies Limite: Child / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article