Study to Compare the Triple ACT AL+AQ With the ACT AL in Cambodia and Vietnam
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Artemether | Small molecule | 20 mg | — |
| Subject | amodiaquine | Other / unclassified | 150 mg | — |
| Subject | lumefantrine | Small molecule | 120 mg | — |
| Background | Primaquine | Small molecule | — | — |