drugset / Trial / NCT03962062
A Pharmacokinetic and Safety Study of Moxidectin to Identify an Optimal Dose for Treatment of Children 4 to 11 Years
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Moxidectin | Other / unclassified | 4 mg | Oral |
| Subject | Moxidectin | Other / unclassified | 6 mg | Oral |
| Subject | Moxidectin | Other / unclassified | 8 mg | Oral |