New drug fights neglected tropical disease
Researchers said Thursday they had successfully tested a Chinese-developed drug against opisthorchiasis, a neglected tropical disease that threatens some 67 million people in Southeast Asia.
Tribendimidine is as safe and effective against the tiny worm that causes the disease as the frontline drug, praziquantel, marketed as Biltricide, they reported in a study published online in the journal Lancet Infectious Diseases.
Opisthorchiasis is caused by a fluke, known by its Latin name as Opisthorchis viverrini, that passes from freshwater snails to river fish, and then to humans if the fish is eaten raw or undercooked.
The fluke holes up in the liver and bile duct, where it reproduces, causing abdominal pain and diarrhoea but also, in the long term, boosting the risk of jaundice, gallstones and cancer.
Around 67 million people in Southeast Asia are at risk from the fluke, and nine million people have already been infected by it, according to a 2005 estimate.
The parasite is endemic to parts of Cambodia, Thailand and Vietnam, but especially in Laos, where as many as 50 percent of schoolchildren and 90 percent of adults are infected.
A team led by Jennifer Keiser from the Swiss Tropical and Public Health Institute randomly assigned 125 infected schoolchildren in Laos' Attepeu province to receiving either tribendimidine, praziquantel or a drug designed to combat the parasite that causes malaria.
Tribendimidine scored the highest cure rate, of 70 percent, followed by praziquantel (56 percent). The three malaria treatments that were taken scored a cure rate of only four percent in two of the drugs and zero in the third.
Both tribendimidine and praziquantel also scored best in clearing the patient of parasite eggs, and were generally well tolerated, with "mild or moderate" side-effects.
The study was a "Phase II" trial in the three-phase process of evaluating a new drug for safety and effectiveness. Wider trials would be needed before it can be licensed internationally for this disease.
(c) 2010 AFP
