Physiologically-Based Pharmacokinetic Models for Optimal Drug Dosing in Children
Physiologically-Based Pharmacokinetic Models for Optimal Drug Dosing in Children
批准号:
8901251
负责人:
Michael Cohen-Wolkowiez
金额:
$67.69万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-08-01 至 2018-06-30
关键词:
AccountingAgeCaringCharacteristicsChildChild DevelopmentChildhoodClindamycinClinical ResearchClinical TrialsClinical Trials DesignCollectionDataDevelopmentDoctor of PhilosophyDoseDrug PrescriptionsDrug usageEnrollmentEnvironmentGeneticGenetic Information Processing PathwayGoalsHealthIndividualInfectionInvestigational New Drug ApplicationLabelLegal patentMedicalMethodologyModelingMonitorNational Institute of Child Health and Human DevelopmentPatientsPharmaceutical PreparationsPharmacologic SubstancePhysiological ProcessesPhysiologyPopulationPrincipal InvestigatorPropertyProtocols documentationPublic HealthPublishingRecording of previous eventsResearchResearch InfrastructureResearch InstituteResearch PersonnelSafetySample SizeSamplingScienceStagingStaphylococcus aureusToxic effectTrainingTreatment FailureTrimethoprim-SulfamethoxazoleValidationbasedata managementdesigndrug developmenteffective therapyexperiencemembermodel developmentpharmacodynamic modelpharmacokinetic modelprospectiveskillstool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The majority of off-patent drugs prescribed to children lack dosing information specific to this population, which can result in treatment failures and toxicities. Dosing information is lacking because clinical trials involving children pose specific challenges, among the most important of which is the large number of children required to estimate appropriate dosing at every stage of child development. Population physiologically based pharmacokinetic (PBPK) models are mathematical tools that incorporate changes of childhood, along with drug characteristics and genetic variances, to find the most appropriate dose for every pediatric age. By incorporating these factors, PBPK models can reduce the number of children needed for clinical trials. This proposal will systematically develop, and prospectively validate, population PBPK modeling in children.
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