About this trial
Tafenoquine was recently approved by regulatory authorities in the USA and Australia. Tafenoquine is an alternative radical curative treatment to primaquine acting against the dormant liver stage of Plasmodium vivax (the hypnozoite). Tafenoquine (an 8-aminoquinoline) has the substantial advantage of single dosing as compared to a 14-day course of primaquine to achieve radical cure. The recommended tafenoquine dose is 300 mg, which was shown to be significantly worse in radical curative efficacy to a total primaquine dose of 3.5 mg/kg in Southeast Asia. The cure rate of tafenoquine 300 mg in Southeast Asian study sites was only 74%. The comparator 3.5 mg/kg total primaquine dose is the standard and most commonly used dose globally, but in Southeast Asia and the Western Pacific, higher doses of primaquine are needed for radical cure. This study aims to determine the optimal dose of tafenoquine in Southeast Asia.
Addendum for Indonesia: The INSPECTOR trial results showed that tafenoquine 300mg was not efficacious for radical cure (79% probability for recurrence after treatment). The comparator arm, low-dose primaquine 3.5mg/kg divided equally over 14 days, showed a 48% probability of recurrence after treatment). The standard of care for radical cure in Indonesia is high-dose primaquine 7mg/kg divided in 7 daily doses).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Patients with symptomatic P. vivax mono-infection as diagnosed by microscopy
Fever or history of fever in the previous 7 days
Quantitative G6PD activity ≥70% of the population median
Weight >10 kg and ≥2 years old
Disqualifiers
Pregnancy
Lactation
Hb < 8 g/dL
Severe malaria
Trial design
Parallel
Treatments tested in this trial
Tafenoquine
DrugTafenoquine will be given as 100mg coated tablets. Tablets will be given based on weight bands.
Chloroquine
DrugChloroquine will be given as daily dose over 3 days (25mg/kg total dose divided 10/10/5mg/kg)
Artemether 20 mg-Lumefantrine 120 mg
DrugArtemether-lumefantrine will be given twice daily over 3 days. Whole tablets will be given based on weight bands.
Primaquine
DrugPrimaquine will be given once daily over 7 days (7mg/kg total dose divided 1mg/kg/day) as per the national malaria guidelines.
Dihydroartemisinin 40 mg-Piperaquine 320 mg
DrugDihydroartemisinin-piperaquine will be given once daily over 3 days. Whole tablets will be given based on weight bands.
Treatment groups
Trial outcomes
Primary outcomes
Microscopy positive P. vivax recurrence after radical treatment up to month 4
Secondary outcomes
Sub-microscopic P. vivax recurrence after radical treatment between day 28 and month 4
Sub-microscopic P. vivax recurrence with very low parasite density after radical cure treatment at days 14 and 21
Number of serious adverse events (e.g., hospitalization for symptomatic hemolysis or methemoglobinemia)
Number of adverse events (e.g., gastrointestinal symptoms)
Sponsors and contacts
Click on the lead sponsor to view all of their trials.