Clinical trial Recruiting at 1 site Phase 3 Interventional

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).

More Lymphatic Filariasis trials

Quick facts

PhasePhase 3
Study typeInterventional
SexAll
Enrollment5100 (estimated)
SponsorMedicines Development for Global Health
Academic / other
Locations1 site (Suva)
StatusRecruiting
StartedSeptember 28, 2026
Main results expectedJune 2027
Study endsJune 2028
Registry record updatedOctober 7, 2026
Trial IDNCT07159373 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

  • Ministry of Health and Medical Services Fiji
    Suva, Fiji
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.