Wenyu Yang, Andrew Steer, Ben Coghlan, Khampheng Phongluxa, Xiao Zhu, Amanda Gwee
{"title":"Ivermectin dosing for children under 2 years.","authors":"Wenyu Yang, Andrew Steer, Ben Coghlan, Khampheng Phongluxa, Xiao Zhu, Amanda Gwee","doi":"10.1093/jac/dkaf344","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Ivermectin is effective against scabies but not licensed for children weighing <15 kg. We aimed to identify an ivermectin dosing strategy for children aged <2 years.</p><p><strong>Methods: </strong>Doses for three age subgroups under 2 years were simulated by incorporating a maturation function for metabolizing enzymes into a population pharmacokinetic (PopPK) model to achieve median plasma AUC0-∞ between 80% and 125% of that observed in children aged 5-15 years receiving the standard 200 μg/kg dose (AUC0-∞ 976 μg/L h). Patient covariates were sampled from the National Health and Nutrition Examination Survey dataset. Final doses were rounded to feasible fractions of a 3 mg tablet.</p><p><strong>Results: </strong>For infants aged 3-7 months, a 0.75 mg dose (one-fourth tablet) resulted in a median AUC0-∞ of 835 μg/L h [IQR: 632-1017]; for 8-12 months, a 1.5 mg dose (one-half tablet) yielded 848 μg/L h [IQR: 774-934]; and for 13-24 months, a 3 mg dose (one tablet) resulted in 1033 μg/L h [IQR: 943-1173]. All doses achieved median exposures within 80%-125% of the reference AUC in older children.</p><p><strong>Conclusions: </strong>A dosing strategy for ivermectin in children aged 3 months-2 years was developed using a CYP3A4 maturation-based PopPK model. This regimen will be evaluated in an upcoming clinical trial to inform safe and effective scabies treatment in young children.</p>","PeriodicalId":14969,"journal":{"name":"Journal of Antimicrobial Chemotherapy","volume":" ","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Antimicrobial Chemotherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jac/dkaf344","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"INFECTIOUS DISEASES","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: Ivermectin is effective against scabies but not licensed for children weighing <15 kg. We aimed to identify an ivermectin dosing strategy for children aged <2 years.
Methods: Doses for three age subgroups under 2 years were simulated by incorporating a maturation function for metabolizing enzymes into a population pharmacokinetic (PopPK) model to achieve median plasma AUC0-∞ between 80% and 125% of that observed in children aged 5-15 years receiving the standard 200 μg/kg dose (AUC0-∞ 976 μg/L h). Patient covariates were sampled from the National Health and Nutrition Examination Survey dataset. Final doses were rounded to feasible fractions of a 3 mg tablet.
Results: For infants aged 3-7 months, a 0.75 mg dose (one-fourth tablet) resulted in a median AUC0-∞ of 835 μg/L h [IQR: 632-1017]; for 8-12 months, a 1.5 mg dose (one-half tablet) yielded 848 μg/L h [IQR: 774-934]; and for 13-24 months, a 3 mg dose (one tablet) resulted in 1033 μg/L h [IQR: 943-1173]. All doses achieved median exposures within 80%-125% of the reference AUC in older children.
Conclusions: A dosing strategy for ivermectin in children aged 3 months-2 years was developed using a CYP3A4 maturation-based PopPK model. This regimen will be evaluated in an upcoming clinical trial to inform safe and effective scabies treatment in young children.
期刊介绍:
The Journal publishes articles that further knowledge and advance the science and application of antimicrobial chemotherapy with antibiotics and antifungal, antiviral and antiprotozoal agents. The Journal publishes primarily in human medicine, and articles in veterinary medicine likely to have an impact on global health.