drugset / Trial / NCT04188301

Safety and Efficacy of IDA for Onchocerciasis

NCT04188301 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

This DOLF study will investigate the safety and effectiveness of IDA treatment in persons with onchocerciasis when it is administered after pre-treatment with ivermectin to clear or greatly reduce microfilariae from the skin and eyes.

Timeline

Start
2019-12-06
Primary completion
2022-03-14
Completion
2022-06-01

Outcome

Mixed primary results

registry analysis (superiority test); IVM + ALB vs IDA x 1 Dose; p = 0.192; NCT04188301 ↗

registry analysis (superiority test); IVM + ALB vs IDA x 3 Doses; p = 0.023; Odds Ratio (OR) 2.23 (95% CI 1.12 to 4.44); NCT04188301 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Albendazole Small molecule 400 mg Oral
Subject Diethylcarbamazine Small molecule 6 mg/kg Oral
Comparator Ivermectin Small molecule 150 ug/kg Oral

Indications