New hope for kids with liver fluke: drug trial launches
NCT ID NCT07262814
First seen Jun 25, 2026 · Last updated Aug 05, 2026 · Updated 5 times
Summary
This study tests different doses of a drug called arpraziquantel in children aged 6-7 who are infected with a liver fluke parasite (Opisthorchis viverrini). The goal is to find the safest and most effective dose to cure the infection. 125 children will receive one of several doses, and researchers will check if the parasite is gone after treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- arpraziquantel (a drug to treat parasitic worm infections)
- What this could lead to
- If successful, this could provide a safe and effective treatment for liver fluke infection in young children, helping to reduce disease burden in affected communities.
- What could go wrong
- This is a small, early-phase trial (Phase 2) with only 125 children. The optimal dose may not be found, or the drug may not work as well as hoped. Side effects are possible.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 125 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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6 to 7 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 6 to 7 years (i.e., 72 to 95 months). * Written informed consent signed by parents/caregivers (signature or thumbprint). * Agree to comply with study procedures, including provision of two stool samples at baseline and at follow-up assessment 21-28 days after treatment, respectively. * Willing to be examined by a study physician prior to treatment. * At least two slides of the quadruple Kato-Katz thick smears positive for O. viverrini. Exclusion Criteria: * Presence or signs of major systemic illness, e.g. severe anaemia (haemoglobin level of \< 80 g/L according to WHO) upon initial clinical assessment. * Known or suspected infection with Taenia solium (cysticercosis). * Known or suspected acute schistosomiasis. * Abnormal liver and kidney function. * Use of anthelminthic drugs within 4 weeks before or during study period. * Known allergy to study medications (i.e. praziquantel or any of the excipients). * Being prescribed or taking concomitantly medication with known contraindication or drug interactions with the study medication. * Concurrent participation in other clinical trials.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Lao Tropical and Public Health Institute (Lao TPHI)
RECRUITINGVientiane, Laos
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