drugset / Trial / NCT03962062

A Pharmacokinetic and Safety Study of Moxidectin to Identify an Optimal Dose for Treatment of Children 4 to 11 Years

NCT03962062

Phase 1 Completed 36 enrolled Medicines Development for Global Health
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary purpose of this study is to determine a dose of moxidectin for children 4 to 11 years that is equivalent to an 8 mg dose administered for treatment of onchocerciasis in people 12 years and over. The secondary purpose is to evaluate the safety and pharmacokinetics of a single dose of moxidectin in children and adolescents aged 4 to 17 years.

Timeline

Start
2021-03-29
Primary completion
2022-05-30
Completion
2022-09-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Moxidectin Other / unclassified 4 mg Oral
Subject Moxidectin Other / unclassified 6 mg Oral
Subject Moxidectin Other / unclassified 8 mg Oral

Indications