Single-dose Malaria Treatment Using Four Drugs Achieves High Cure Rates In Clinical Trial

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Hundreds of malaria patients participating successful a Phase 3 objective proceedings successful Gabon successful West Africa were cured via a azygous dose of a curen that utilizes 4 wide disposable malaria drugs, according to a caller study presented coming astatine nan Annual Meeting of nan American Society of Tropical Medicine and Hygiene (ASTMH).

The beforehand addresses a brace of problems that person contributed to a stalled conflict against a illness that each twelvemonth kills astir 600,000 people: nan alarming emergence of drug-resistant malaria and nan truth that a 3rd aliases much of malaria patients neglect to complete nan modular three-day people of treatment, which tin some promote supplier guidance and let curable cases to intensify. 

We recovered that our single-dose curen was conscionable arsenic effective arsenic nan modular people that typically requires taking six doses spaced retired complete 3 days, which galore patients ne'er complete."

Ghyslain Mombo-Ngoma, MD, PhD, lead writer of nan study and caput of objective operations, Medical Research Center of Lambaréné, Gabon (known by its French acronym CERMEL)

He noted nan single-dose curen combining sulfadoxine, pyrimethamine, artesunate and pyronaridine (SPAP) whitethorn beryllium much effective against drug-resistant parasites than modular therapies because nan caller operation of 4 medicines-versus 2 narcotics typically utilized successful accepted treatments-targets 4 different vulnerabilities successful nan malaria parasite. Mombo-Ngoma said forcing a pathogen to conflict a multi-front conflict has been utilized to antagonistic supplier resistant tuberculosis and is of increasing liking to malaria experts. Meanwhile, he said a single-dose action for treating malaria addresses nan problem of guidance emerging successful patients that don't complete their afloat people of medicines-while besides curing cases that, if insufficiently medicated, tin let malaria to persist and perchance origin life-threatening complications.

There is an urgent request for caller ways to dainty malaria patients because successful sub-Saharan Africa, which accounts for 95% of nan world's malaria infections and deaths, nan conflict against nan illness has deed a plateau. After falling dramatically from 2000 to 2015, malaria infections and deaths, which chiefly hap successful children nether 5 years old, person increased. The astir caller figures disposable from nan World Health Organization show that successful 2023, location were 263 cardinal cases and 597,000 deaths, compared pinch 2016 levels of 216 cardinal cases and 445,000 deaths. 

Along pinch backing threats, a cardinal impediment to rejuvenating nan fight against malaria is that parasites are processing astatine slightest partial guidance to treatments that harvester artemisinin-based malaria narcotics (once hailed arsenic a awesome breakthrough against malaria) pinch 1 different medicine.

"Another situation is that artemisinin operation therapies (ACTs) must beryllium taken for 3 days to clear parasites from infected patients, and a 3rd aliases much of malaria patients don't complete nan afloat course," Mombo-Ngoma said. He said this nonaccomplishment tin let a ample number of parasites to linger successful nan body, posing nan consequence that they could proceed to multiply and origin terrible disease, while besides giving them clip to create mutations that tin flooded ACTs.

One dose to conflict 2 malaria foes: Treatment adherence and supplier resistance

Mombo-Ngoma and his colleagues, who see Peter Kremsner, MD, PhD, head of nan Institute of Tropical Medicine astatine Germany's University of Tübingen, precocious published an study successful nan Malaria Journal that made nan lawsuit for fighting nan copy problems of curen adherence and supplier guidance by attempting to cure patients pinch a azygous dose comprised of respective different malaria medications, each of them easy accessible successful sub-Saharan Africa. They besides person been moving to trial nan attack successful patients. From May 2024 to October 2025, they led a squad that conducted a proceedings successful Gabon involving treating much than 1,000 patients, half of them nether 10 years old, who were fighting what is known arsenic "uncomplicated malaria." That intends they were sick, but they were not yet suffering terrible life-threatening symptoms.

A small complete half of nan patients (539) were treated pinch a regimen that progressive administering a azygous dose consisting of 2 different malaria "combination" medicines, which together impact 4 different drugs. One is known arsenic SP, because it utilizes nan narcotics sulfadoxine and pyrimethamine, and nan different is called AP, because it employs artesunate (which is simply a type of artemisinin) alongside pyronaridine. The remainder of nan patients (442) received a wide utilized ACT that combines nan artemisinin supplier artemether pinch lumefantrine, aka AL, which requires taking six doses complete 3 days.

Blood tests conducted 28 days aft nan treatments showed that 93% of patients who received nan single-dose cure were free of parasites compared to 90% who sewage nan modular three-day course-meaning they were fundamentally arsenic effective. Mombo-Ngoma said location were nary reports of study supplier related superior adverse events successful immoderate of nan patients.

"Another cardinal advantage is that our single-dose cure was accomplished pinch narcotics that are presently disposable to malaria curen programs crossed Africa-and comparatively affordable arsenic well," he said. "One of nan medications, nan sulfadoxine-pyrimethamine (SP) combination, is simply a generic supplier already manufactured successful respective African countries, while artesunate-pyronaridine (AP) is not yet disposable arsenic a generic but will beryllium by early 2026."

Mombo-Ngoma said location are already discussions underway pinch a supplier shaper to nutrient SP and AP arsenic a azygous capsule aliases sachet (a packet of pills). He besides said malaria researchers successful Mali, Ghana, Kenya and Mozambique person expressed liking successful testing nan single-dose approach.

The grounds supporting a single-dose cure that could astatine slightest trim nan threat of supplier guidance is arriving astatine a clip of encouraging advancement successful processing caller compounds tin of defeating drug-resistant parasites. Mombo-Ngoma noted that while location is dream connected nan horizon, moreover successful a best-case scenario, it will still return respective years for nan astir precocious of these compounds to go wide disposable successful Africa.

"I'm a malaria researcher, but I'm besides a expert treating a batch of malaria patients, and I request caller options now," he said. "What I dream is that, if we proceed to person occurrence pinch this single-dose cure, it tin service arsenic a span to nan caller treatments now nether development-something we tin deploy very soon while we await nan presence of different options."

"It's breathtaking to spot our members pursuing innovative ways of fighting drug-resistant malaria while besides seeking solutions to treatment-adherence challenges, which is simply a pervasive problem successful nan guidance of galore diseases," said ASTMH President David Fidock, PhD, who heads a group of experts connected antimalarial supplier guidance that advises nan WHO Malaria and Neglected Tropical Diseases Program. "This study is besides a reminder that, astatine a clip erstwhile nan full section of world wellness is facing tremendous headwinds, ASTMH members are keeping their attraction connected investigation that tin support amended wellness for millions of group successful low- and middle-income countries." 

Source:

Journal reference:

Mombo-Ngoma, G., et al. (2025). Making nan astir of existing antimalarial medicines: a azygous dose cure pinch sulfadoxine–pyrimethamine positive artesunate–pyronaridine. Malaria Journal. doi: 10.1186/s12936-025-05559-4. https://malariajournal.biomedcentral.com/articles/10.1186/s12936-025-05559-4

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