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sevuparin sodium + atovaquone + proguanil
- Development stage
- Unknown
- Lead developer
- Modus Therapeutics
- Modality
- Small Molecules
- Administration
- Intravenous, Oral
01
Overview
This is a combination of three agents: sevuparin sodium, atovaquone, and proguanil. Atovaquone and proguanil are antimalarial drugs used together to treat and prevent malaria caused by *Plasmodium falciparum*. Atovaquone inhibits the mitochondrial electron transport chain in the parasite, while proguanil acts as a biguanide that enhances the effect of atovaquone on mitochondrial membrane potential; its metabolite cycloguanil also inhibits dihydrofolate reductase but this is not central to their synergy[1][6]. Sevuparin sodium is an experimental drug being studied as an adjunctive therapy for severe malaria; it is a modified heparinoid designed to block sequestration of infected red blood cells in microvasculature, potentially improving outcomes when combined with standard antimalarial therapies[4]. The triple combination has been investigated for improved efficacy against severe or complicated malaria.
- Brand names
- Malarone
- Other names
- atovaquone and proguanil hydrochloridesevuparin/DF02
02
Targets
bc1 complex (Cytochrome bc1 complex (plasmodium))PfEMP1 (Plasmodium falciparum erythrocyte membrane protein 1)DHFR (Dihydrofolate reductase)
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