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Filling the gaps: expanding malaria treatments for those without options

What it is

Pyramax® and Eurartesim® are two established antimalarial medicines whose safety and efficacy have been progressively expanded through EDCTP-supported research to reach more patient groups who lack specific treatments, such as children, pregnant women, and patients requiring re-treatment.

Why it matters

Malaria is a leading cause of child mortality in Africa, and treatment options remain insufficient for many priority populations. Extending proven medicines to new groups is as important as developing new ones. By supporting the generation of this evidence, EDCTP has helped ensure that more people can access safe, effective treatment.

The story

Each year, malaria affects more than 250 million people and causes over half a million deaths, the majority among children under five.[1] Since 2003, EDCTP has supported over 20 malaria research projects,[2] advancing simpler and improved therapies for children with severe malaria[3] and for pregnant women.[4]

EDCTP-supported research has contributed to broadening the reach of two important antimalarial medicines:

Pyramax® (pyronaridine tetraphosphate and artesunate) js a medicine used to treat uncomplicated malaria, caused by two types of malaria parasites, Plasmodium falciparum and Plasmodium vivax. In 2012, it was approved as an effective antimalarial treatment[5] by the European Medicines Agency (EMA). EDCTP has since supported studies  to reconfirm its safety and efficacy for re-treatment,[6]expand its label to include pregnant women,[7] and facilitate the development of a paediatric formulation.[8] These efforts have progressively strengthened the evidence base, enabling its use for the populations that need it most.

Eurartesim® (piperaquine tetraphosphate and artenimol) is a fixed-dose artemisinin-based combination therapy. With EDCTP funding, researchers conducted clinical trials to assess its safety, optimal dosing, and side effects in vulnerable groups, including young children across sub-Saharan Africa.[9]

These studies generated evidence that informed World Health Organization (WHO) recommendations and strengthened the evidence base for Eurartesim®, supporting its approval by the European Medicines Agency as a treatment option for uncomplicated malaria.[10]

Today, it is widely used across Africa and Asia and has been adopted as a second-line therapy in countries such as Ghana, where it continues to show efficacy rates above 90% in children under routine use.[11]

Global Health EDCTP3 continues to drive innovation against malaria, including supporting new formulations to address drug resistance,[12] protect pregnant women,[13] and improve vector-control tools.[14]

 

Sources:

[1] Malaria

[2] Malaria – International partnerships against infectious diseasesand Malaria treatment – EDCTP

[3] Simplified artesunate regimen found efficacious in treating children with severe malaria – EDCTP

[4] PREGACT: Safety and efficacy of four artemisinin-based combination treatments in African pregnant women with malaria – EDCTP

[5] Pyramax – opinion on medicine for use outside EU | European Medicines Agency (EMA)

[6] Re-treating malaria with Pyramax®: WANECAM study supports safety and efficacy – EDCTP

[7] Pyramax® label update: Now includes information for the treatment of pregnant women with malaria | Medicines for Malaria Venture

[8] Pyramax® approved as antimalarial for treatment of multiple episodes of malaria – EDCTP

[9] Malaria treatment: The 4ABC study

[10] European Medicines Agency recommends new malaria treatment for approval | European Medicines Agency (EMA)

[11] Abuaku B, Boateng P, Peprah NY, Asamoah A, Duah-Quashie NO, Matrevi SA, Amoako EO, Quashie N, Owusu-Antwi F, Malm KL and Koram KA (2023) Therapeutic efficacy of dihydroartemisinin-piperaquine combination for the treatment of uncomplicated malaria in Ghana. Front. Cell. Infect. Microbiol. 12:1058660. doi: 10.3389/fcimb.2022.1058660

[12] WANECAM-2 consortium reports positive results from phase 2b study of novel treatment for children with malaria

[13] Home – SAFIRE – Safety of Antimalarials in FIRst trimEster

[14] DEFEND and LASR