drugset / Trial / NCT01082705

Assessing the Efficacy of Artemisinin Combination Therapies for Treatment of Uncomplicated Malaria Infection in Children

NCT01082705

Phase 3 Completed 323 enrolled Centers for Disease Control and Prevention
RandomizedParallel-groupOpen-labelTreatment

Summary

Following the rapid development of significant drug resistance to both chloroquine and sulfadoxine-pyrimethamine (the first line therapy in Tanzania from 2001 -2006), artemether- lumefantrine (Coartem or AL) was adopted as first line therapy in Tanzania in 2006. Now that this drug has been widely used for some time, the investigators propose to conduct an antimalarial efficacy trial to monitor the effectiveness of this therapy, to determine if this drug remains efficacious, or if significant resistance has emerged, in which case a new antimalarial strategy will need to be contemplated. The investigators hypothesize that the efficacy of Artemether-lumefantrine remains high, and that the other artemisinin combination therapies will be equally efficacious. Children 6-59 months of age with symptomatic malaria will be randomly assigned to be treated with either artemether + lumefantrine (Coartem) or dihydroartemisinin-piperaquine (Duo-Cotecxin or Artekin). Clinical, parasitologic, and hematologic parameters will be monitored over a 42-day follow-up period and will be used to evaluate drug efficacy.

Timeline

Start
2010-04
Primary completion
2011-06
Completion
2011-06

Drugs

EvaluationDrugModalityDoseRoute
Subject ARTENIMOL Small molecule 6.4 mg/kg
Comparator Artemether Small molecule 20 mg
Comparator Artemether Small molecule 40 mg
Comparator Artemether Small molecule 60 mg
Comparator Artemether Small molecule 80 mg
Comparator lumefantrine Small molecule 120 mg
Comparator lumefantrine Small molecule 240 mg
Comparator lumefantrine Small molecule 360 mg
Comparator lumefantrine Small molecule 480 mg
Subject piperaquine Small molecule 51.2 mg/kg