Use of Modeling and Simulation in the Design and Conduct of Pediatric Clinical Trials and the Optimization of Individualized Dosing Regimens
Author:
Affiliation:
1. Department of PediatricsUniversity of Utah School of MedicineSalt Lake City Utah USA
2. SanofiPhiladelphia Pennsylvania USA
Publisher
Wiley
Subject
Pharmacology (medical),Modelling and Simulation
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/psp4.12038
Reference66 articles.
1. Practical Considerations for Dose Selection in Pediatric Patients to Ensure Target Exposure Requirements
2. Adolescent Dosing and Labeling Since the Food and Drug Administration Amendments Act of 2007
3. Clarification on Precision Criteria to Derive Sample Size When Designing Pediatric Pharmacokinetic Studies
4. Sample Size Calculations Based on Generalized Estimating Equations for Population Pharmacokinetic Experiments
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