New malaria drug shows promise in severe cases
NCT ID NCT04675931
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a new intravenous drug called cipargamin in 254 adults and children with severe malaria. The goal was to find a safe and effective dose that quickly clears the malaria parasite, especially in areas where standard treatments are becoming less effective. Researchers measured how well the drug reduced parasite levels and improved clinical outcomes within 48 hours.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cipargamin (KAE609)
- What this could lead to
- If successful, cipargamin could offer a new treatment option for severe malaria, especially where current drugs are losing effectiveness due to resistance.
- What could go wrong
- This is a Phase 2 trial with only 254 participants, so results are preliminary. The drug may not prove safe or effective in larger studies, and side effects are still being evaluated.
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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254 people
The number who actually took part.
- Started
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Mar 2022
- Finished
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Aug 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
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 months to 100 years
- 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.
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: * Cohort 1: Participants aged ≥ 12 years with moderately severe malaria as defined in (prostration and/or repeated vomiting) without presence of other signs of severe malaria (and with high P. falciparum parasitemia (60,000-250,000 parasites per µl) * Subsequent Cohorts 2 to 5: Participants diagnosed with severe malaria as defined in modified version of WHO criteria and P. falciparum parasite count of ≥ 5000 per µl * Cohort 2: Participants aged ≥ 12 years * Cohort 3: Participants aged 6 - \< 12 years * Cohort 4: Participants aged 2 - \< 6 years * Cohort 5: Participants aged ≥ 6 months - \< 2 years Exclusion Criteria: Exclusion criteria applying to all Cohorts 1 to 5: * Mixed Plasmodium infections * Treatment with quinine or artemisinin derivative or any other antimalarial drug or any antibiotic with known antimalarial activity within 12 hours of screening. * Signs/symptoms of severe malnutrition in general accordance with WHO guidelines: 1. Under 18 years: \<-3 Z-scores of WHO growth standard for weight-for-height/length (in children \< 5 years) or BMI for age (5-18 years), or very low mid-upper arm circumference (MUAC \< 115 mm in children \< 12 years, \< 160mm 12-18 years), or bilateral pitting edema 2. Over 18 years: BMI \< 16 kg/m2 or MUAC \< 160mm or bilateral pitting edema * Known underlying illness, surgical or medical condition, which is not related to ongoing event of severe malaria and which might jeopardize the participant's health in case of participation in the study or which might alter the distribution, metabolism or excretion of study treatment. For example: 1. neurological or neurodegenerative disorders, 2. cardiac, renal, or hepatic disease, diabetes, 3. epilepsy, cerebral palsy, 4. known or suspected to be HIV-1 positive and/or receiving antiretroviral treatment 5. malignancy of any organ system (other than localized basal cell carcinoma of the skin or in situ cervical cancer), treated or untreated, within the past 5 years, regardless of whether there is evidence of local recurrence or metastases 6. known or suspected cases of active infections or concurrent febrile illness such as TB, Typhoid, COVID-19 etc. Additional exclusion criteria are as follows: Exclusion criteria for Cohort 1: * ALT \> 5 x the upper limit of normal range (ULN), regardless the level of total bilirubin * Total bilirubin is \> 3 mg/dL * Body weight of \< 35 kg or \>75 kg Exclusion criteria for Cohort 2: * Body weight of \< 35 kg or \>75 kg * Participants diagnosed as moderately severe malaria due to repeated vomiting without presence of any of the symptoms of severe malaria Exclusion criteria for Cohorts 3 to 5: * Body weight of \< 5 kg * Participants diagnosed as moderately severe malaria due to repeated vomiting without presence of any of the symptoms of severe malaria
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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
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Novartis Investigative Site
Burkina Faso, 2208, Burkina Faso
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Novartis Investigative Site
Ouagadougou, Burkina Faso
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Novartis Investigative Site
Abidjan, 13BP972, Côte d’Ivoire
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Novartis Investigative Site
Agboville, BP 154, Côte d’Ivoire
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Novartis Investigative Site
Kinsasha, Democratic Republic of Congo, BP 7948, Democratic Republic of the Congo
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Novartis Investigative Site
Siaya, 2300, Kenya
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Novartis Investigative Site
Manhiça, Maputo Province, 1929, Mozambique
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Novartis Investigative Site
Kigali, BP 4560, Rwanda
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Novartis Investigative Site
Tororo, 10102, Uganda
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