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| Funder | European Commission |
|---|---|
| Recipient Organization | Bernhard-Nocht-Institut Fuer Tropenmedizin |
| Country | Germany |
| Start Date | Jan 01, 2024 |
| End Date | Dec 31, 2025 |
| Duration | 730 days |
| Number of Grantees | 7 |
| Roles | Participant; Coordinator |
| Data Source | European Commission |
| Grant ID | 101145769 |
Susceptibility to Artemisinin-based combination therapies (ACTs) currently remains high among the African Plasmodium falciparum population, but resistant mutant has been detected recently.
To mitigate the risk of resistance leading to a dramatic increase in malaria related mortality, more efficient ACTs need to be urgently explored for quick deployment in Africa.
Artemether-lumefantrine (AL) is widely used and shows high efficacy and favourable safety in Africa but needs to be protected to increase its useful lifespan. Atovaquone-proguanil (AP) is highly efficacious, safe and resistant parasites are not circulating in any endemic area.
AP targets multiple parasite stages -liver and blood in human host, and mosquito- through an independent mode of action, limiting the risk of cross-resistance with current ACTs.The aim of the project is to assess the efficacy of a triple-therapy associating artemether-lumefantrine (AL) and atovaquone-proguanil (AP) for the treatment of uncomplicated P. falciparum malaria in African children in a non-inferiority comparator-controlled trial.A phase III clinical trial will be conducted to compare safety and cure rate of a 3-day treatment course with AL+AP versus AL in 1,664 consenting 6 to 70 months children with uncomplicated malaria from Benin, Gabon, Ghana and Mali.
The main outcome will be cure rate at day-42, excluding reinfections.
Antimalarial pharmacokinetic parameters and post-treatment prophylactic efficacy will be estimated for the two treatments and compared.
Sub-studies will look at transmission-blocking efficacy through membrane-feeding assays and gametocyte dynamics, drug resistance selection.By proofing that AL+AP has safety and cure rate similar to AL, this project will lead to important public health-level benefits by provision of a first candidate regimen to be deployed when ACT resistance spreads throughout Africa and by decreasing human to mosquito transmission.
Universite Des Sciences Des Techniques Et Des Technologies de Bamako; Kwame Nkrumah University of Science and Technology Kumasi; Institut de Recherche Clinique Du Benin (Ircb); Institut Des Sciences Et Techniques; Bernhard-Nocht-Institut Fuer Tropenmedizin; Institut de Recherche Pour Le Developpement; Centre de Recherches Medicales de Lambaréné
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