Malaria drugs under watch: resistance study in kenya
NCT ID NCT07362498
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study in western Kenya looked at how well different malaria drugs work and whether the parasites are becoming resistant. Researchers tested four artemisinin-based combination therapies across 28 health facilities over 28 months, involving 316 people with uncomplicated malaria. The goal was to see if using multiple first-line treatments is practical and acceptable, and to track resistance markers in the malaria parasite.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Artemether + Lumefantrine and Dihydroartemisinin-piperaquine
- What this could lead to
- If successful, this could help health officials choose the best combination of malaria drugs to slow down resistance and keep treatments effective longer.
- What could go wrong
- This is an observational study, not a test of a new cure. The findings may not apply to other regions, and drug resistance patterns can change over time.
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.
- Participants
-
316 people
The number who actually took part.
- Started
-
Jun 2020
- Finished
-
Jan 2024
- Lead sponsor
-
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.
Who is studied
Patients diagnosed with uncomplicated Plasmodium falciparum malaria at participating government and faith-based health facilities in Homa Bay County and Migori County, Western Kenya, a malaria-endemic region with high transmission intensity.
- Ages
-
5 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 5 years or older * Clinical diagnosis of uncomplicated malaria * Confirmed Plasmodium falciparum infection by rapid diagnostic test (RDT) or microscopy * Presenting at participating health facility for malaria treatment * Able and willing to provide informed consent (or parental/guardian consent for minors under 18 years) * Resident of study catchment area * For molecular surveillance substudy: willingness to provide dried blood spot sample Exclusion Criteria: * Pregnant women (due to contraindications for some study medications in first trimester and lack of safety data) * Children under 5 years of age (due to lack of pediatric formulations for some study medications) * Severe or complicated malaria requiring parenteral treatment or hospitalization * Known hypersensitivity or contraindication to any of the study artemisinin-based combination therapies * Unable to take oral medications * Previous participation in current treatment episode (repeat visits) * Concurrent participation in other interventional malaria treatment studies
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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.
Contacts and locations
Locations
-
Homa Bay County Health Facilities
Homa Bay, Homa Bay County, 40300, Kenya
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Migori County Teaching and Referral Hospital
Migori, Migori County Kenya, 40400, Kenya
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Other studies related to the condition(s) this trial covers.
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