About this trial
Plasmodium vivax is the most geographically widespread malaria species and the second largest contributor to symptomatic malaria worldwide. It accounts for half of all malaria cases outside Africa, with an estimated 14.3 million clinical vivax malaria cases reported annually, contributing to an annual cost of US$359 million. Children are most vulnerable to infection, with P. vivax prevalence peaking between 2 to 6 years of age. In Papua New Guinea (PNG), there are \>1.5 million suspected P. vivax cases annually, and while P. falciparum infections are the most prevalent, P. vivax transmission is the most intense in the world. P. vivax in PNG provides a unique epidemiological setting in which to assess innovative treatments in children.The complex biology of P. vivax represents a challenge for malaria control and chemotherapy, especially dormant liver-stage parasites (hypnozoites) which can reactivate (relapse) and cause disease at a time remote from the primary infection. Hypnozoite relapse is the primary cause of vivax malaria in endemic regions and is resistant to most antimalarial drugs. Identifying effective treatments for radical cure, the complete elimination of parasites (both blood- and liver-stage), is therefore a priority. The World Health Organization (WHO) recommends a 14-day radical cure regimen for uncomplicated vivax malaria; comprised of blood stage treatment (chloroquine or artemisinin combination therapy (ACT)) and 14 days of the 8-aminoquinoline drug primaquine (PQ; 0.25-0.5 mg/kg/day) for liver-stage cure. More recently, the 8-aminoquinoline tafenoquine has garnered interest as an alternative radical cure agent to primaquine. However, there is limited data on the pharmacokinetics, tolerability and radical cure efficacy of tafenoquine in children. Furthermore, early data suggest a drug interaction between TQ and artemisinin combination therapy (ACT) drugs - which requires further investigation and confirmation. This study will generate critical paediatric safety, tolerability, pharmacokinetic, and preliminary efficacy data for TQ when administered with either artemether-lumefantrine or dihydroartemisinin-piperaquine in PNG children with uncomplicated malaria.
Eligibility criteria
Qualifiers
Have normal G6PD activity (>70% enzyme activity) as confirmed by quantitative SD Biosensor
Do not have severe malaria (by WHO criteria)
Have rapid diagnostic test and/or microscopically confirmed uncomplicated malaria (any species)
Have no significant co-morbidity
Disqualifiers
Have <70% G6PD enzyme activity, as confirmed by quantitative SD Biosensor
Have signs or symptoms of severe malaria (by WHO criteria)
Test negative for malaria by rapid diagnostic test and/or microscopy
Have signs or symptoms of a significant co-morbidity
Trial design
Treatments tested in this trial
- Single dose tafenoquine (10 mg/kg)
- Dihydroartemisinin-piperaquine (DHA-PPQ)
- Artemether + Lumefantrine
Treatment groups
Sponsors and collaborators
Curtin University
Lead sponsor
Papua New Guinea Institute of Medical Research
Collaborator
The University of Western Australia
Collaborator