Better options for treating lymphatic filariasis and other infections in communities
Official title: Safety and Efficacy Trial of Mass Drug Administration With Moxidectin Versus Ivermectin in Combination With Diethylcarbamazine and Albendazole for Lymphatic Filariasis, Scabies, and Strongyloidiasis in Fiji
Run by Medicines Development for Global Health · NCT07159373 · Data updated 2026-11-12
This trial tests whether a three-drug regimen (moxidectin, diethylcarbamazine, and albendazole) can clear lymphatic filariasis, scabies, and strongyloidiasis in people in affected communities, compared with the standard regimen (ivermectin, DEC, and albendazole).
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Sex | All |
| Enrollment | 5100 (estimated) |
| Sponsor | Medicines Development for Global Health Academic / other |
| Locations | 1 site (Suva) |
| Status | Recruiting |
| Started | September 28, 2026 |
| Main results expected | June 2027 |
| Study ends | June 2028 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07159373 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are children and adults living in study locations who are infected or at risk for lymphatic filariasis, scabies, or strongyloidiasis and can provide informed consent.
✕Probably not a fit
Participants with severe illness or allergies to study drugs, or those outside the village-specific eligibility criteria, may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a Phase 3, interventional study evaluating mass drug administration in communities where lymphatic filariasis, scabies, and strongyloidiasis are common. Participants receive three single doses of either MoxDA or IDA, each spaced about a year apart, and are monitored for safety after each treatment. Researchers test participants for the targeted infections at enrollment and follow up with safety checks in the week after each dose. The study compares infection clearance and safety between the MoxDA and IDA regimens.
Why it matters
Potential benefit: If successful, the MoxDA regimen could offer improved infection clearance with an acceptable safety profile for communities affected by these diseases.
How similar studies have gone: Previous studies in similar settings have explored MoxDA and IDA approaches, with ongoing evaluation of safety and efficacy.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Provision of signed and dated informed consent. 2. Resident in one of the study locations. Exclusion Criteria: There are no exclusion criteria to participation in the study. Treatment Exclusion Criteria: Participants are ineligible to receive the treatment regimen allocated to their village if they meet any of the following criteria: 1. Severe illness (any illness that is severe enough to interfere with activities of daily living); 2. Known or suspected allergy to ivermectin, moxidectin, diethylcarbamazine or albendazole; 3. Pregnant; 4. Breastfeeding a baby within 7 days of birth; 5. Age \< 4 years for villages randomised to moxidectin, diethylcarbamazine, and albendazole (MoxDA); or 6. Age \< 2 years or weight \< 15 kg for villages randomized to ivermectin, diethylcarbamazine and albendazole (IDA).
Where it's running
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Ministry of Health and Medical Services Fiji
Suva, Fiji Recruiting
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.