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Completed HORIZON European Commission

Clinical evaluation of AntimalarialS tri-therapy with AtovAquone-Proguanil for treatment of uncomplicated malaria in African children

€1.5M EUR

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
Grant Description

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.

All Grantees

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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