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One pill to stop malaria? new combo shows promise

NCT ID NCT05974267

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether a single dose of two antimalarial drugs, M5717 and pyronaridine, can clear the malaria parasite from the blood and prevent new infections in people who have the parasite but no symptoms. 192 adults and adolescents in malaria-endemic areas took part. The goal is to find a simple, effective way to prevent malaria with just one treatment.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
M5717 and pyronaridine (antimalarial drugs)
What this could lead to
If successful, this could lead to a simple, single-dose preventive treatment for malaria, reducing the need for multiple doses.
What could go wrong
This is an early Phase 2 trial with only 192 participants, so results may not apply to everyone. The combination may not provide long-lasting protection or could have side effects.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

192 people

The number who actually took part.

Started

Nov 2023

Finished

Dec 2024

Lead sponsor

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

12 to 55 years

Sex

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Participants with Asymptomatic Plasmodium falciparum Malaria with no Fever or other sign of Acute Uncomplicated Malaria and, with Microscopic confirmation using Giemsa-stained thick film, and a Parasitemia of \>= 40 to \<= 10,000 Asexual Parasites/Microliter (μL) of Blood. * Axillary Temperature \< 37.0 degree Celcius (ºC) or oral/Tympanic/rectal Temperature\< 37.5ºC; without history of fever during the previous 48 hours. * Have a body weight \>= 45 kilogram (kg) * Participants capable of giving Signed Informed consent which includes Compliance with the requirements and restriction listed in the Informed consent form * Other Protocol defined Inclusion Criteria could apply Exclusion Criteria: * Participants with any disease requiring Chronic Treatment * Participants with any Preplanned surgery during the study * Participants with any previous Treatment with pyronaridine as part of a combination therapy during the last 3 months * Participants with any adequate Hematological, Hepatic, and renal function as defined in the Protocol * Other protocol defined Exclusion Criteria could apply

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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

  • Groupe de Recherche Action en Sante (GRAS)

    Ouagadougou, Burkina Faso

  • Kisumu County Referral Hospital

    Kisumu, Kenya

  • MRC Unit The Gambia at LSHTM

    Banjul, The Gambia

  • Ndola Teaching Hospital

    Ndola, Zambia

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