drugset / Trial / NCT04704999

Southeast Asia Dose Optimization of Tafenoquine

NCT04704999

Phase 4 Recruiting 700 enrolled University of Oxford
RandomizedParallel-groupSingle-blindTreatment

Summary

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.

Timeline

Start
2024-07-22
Primary completion
2027-10-04
Completion
2028-02-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Tafenoquine Small molecule 100 mg
Comparator Tafenoquine Small molecule 150 mg
Comparator Tafenoquine Small molecule 200 mg
Comparator Tafenoquine Small molecule 300 mg
Comparator Tafenoquine Small molecule 450 mg
Background Artemether-lumefantrine Unknown 20 mg
Background Artemether-lumefantrine Unknown 120 mg
Comparator Chloroquine Small molecule 25 mg/kg