Transactions of the Royal Society of Tropical Medicine and Hygiene · 2000 · 156 citations · 17 references
PharmacyPharmacologyPharmacotherapyClinical PharmacologyPediatric Clinical PharmacologyPediatric PharmacotherapyAntiparasitic PharmacologyEssential MedicinesMalariaPediatric Clinical TrialsPediatric PharmacologyTropical MedicineAntimalarial AgentsAntimalarial Drug CombinationsChemotherapy Of MalariaDose Regimen SelectionMedian Effective DosePlasmodium FalciparumTotal DoseTreatment Of Malaria
The efficacy and safety of the 6-dose regimen of artemether-lumefantrine were assessed in an open randomized trial in children and adults presenting with acute, uncomplicated Plasmodium falciparum malaria in Thailand between November 1997 and March 1998. 200 patients were enrolled in 2 centres: 150 received artemether-lumefantrine (i.e., a median total dose of 9.6 mg/kg [interquartile range 8.7-10.7] and 57.9 mg/kg of lumefantrine [52.4-64.0]) and 50 the standard combination of artesunate (12 mg/kg over 3 d) and mefloquine (25 mg/kg). All patients had rapid initial clinical and parasitological responses. The 28 d cure rates were high: 97.7% (95% confidence interval [95% CI] 93.5-99.5%) for artemether-lumefantrine and 100% (95% CI 92.5-100%) for artesunate-mefloquine. The 6-dose regimen of artemether-lumefantrine was better tolerated than, and as effective as, artesunate-mefloquine, the current standard treatment in this area of multidrug-resistant P. falciparum malaria.
17
François Nosten, Michèle van Vugt, Ric N. Price et al. · The Lancet · 2000 · 507 citations
Effects of artemisinin derivatives on malaria transmissibility
Ric N. Price, François Nosten, C. Luxemburger et al. · The Lancet · 1996 · 465 citations