By  Keith Brannon for Futurity.

A new drug is effective against non-severe cases of malaria, clearing the parasite responsible for the disease within a week, a new study reports.

The results are significant as public health experts have long warned that the parasite responsible for most malaria cases, Plasmodium falciparum, is developing resistance to widely used treatments. New medications are needed to build up secondary defenses against drug-resistant strains of the parasite.

The drug, called AQ-13, matches the effectiveness of the most widely used treatment regimen, says Donald Krogstad, professor of tropical medicine at Tulane University School of Public Health and Tropical Medicine.

“The clinical trial results are extraordinarily encouraging. Compared to the current first-line recommendation for treatment of malaria, the new drug comes out very well.”

Mosquitoes infected by a parasite spread malaria, causing more than 200 million illnesses across the globe and more than 400,000 deaths annually. For decades, chloroquine was used to treat malaria until Plasmodium falciparum developed resistance.

“The potential long-term implications are bigger than one drug…if you understand the resistance well enough, you may be actually be able to develop others as well.”

Now, a drug combination—artemether and lumefantrine—is the primary treatment for malaria although resistance is also developing to the drug combination in some countries.

For the new study in The Lancet Infectious Diseases, researchers recruited 66 adult men in Mali with uncomplicated malaria, which is defined as malaria that isn’t life threatening. Half were treated with AQ-13 and the other half received artemether and lumefantrine.

Both drug groups had similar cure rates. However, five participants in the AQ-13 group left the study or were lost to follow-up and two participants in the artemether/lumefantrine group had late treatment failures with recurrence of their original infections.

Researchers hope to expand testing of the drug to more participants, including women and children, before it can be widely recommended as a new treatment.

The same biotechnology that helped the team develop the new drug has also identified similar drugs that also hold promise against drug-resistant parasites, Krogstad says.

“The potential long-term implications are bigger than one drug. The conceptual step here is that if you understand the resistance well enough, you may be actually be able to develop others as well.”

Other researchers from Tulane and from the University of Bamako are coauthors of the study.

Source: Tulane University

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