drugset / Trial / NCT03355664

Study to Compare the Triple ACT AL+AQ With the ACT AL in Cambodia and Vietnam

NCT03355664

Phase 3 Completed 310 enrolled University of Oxford
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a multi-centre, open-label randomised trial to assess the efficacy, safety and tolerability of the Triple ACT artemether-lumefantrine+amodiaquine (AL+AQ) compared to the ACT artemether-lumefantrine (AL) in uncomplicated falciparum malaria in Cambodia and Vietnam. The estimated total sample size is 600 patients from 2 sites in Cambodia and 2 sites in Vietnam. There are 2 treatment arms Arm 1: Artemether-lumefantrine for 3 days Arm 2: Artemether-lumefantrine for 3 days plus Amodiaquine for 3 days. According to the World Health Organization guideline, all patients except children under 10 kilograms will also be treated with a single dose of primaquine as a gametocytocidal treatment. Funder :Bill \& Melinda Gates Foundation (BMGF) Grant reference number: OPP1132628

Timeline

Start
2018-03-19
Primary completion
2020-03-04
Completion
2020-03-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Artemether Small molecule 20 mg
Subject amodiaquine Other / unclassified 150 mg
Subject lumefantrine Small molecule 120 mg
Background Primaquine Small molecule