Southeast Asia Dose Optimization of Tafenoquine

Recruiting Phase 4 Interventional Study
Plasmodium Vivax Malaria
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
2 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
820 (estimated)
Sponsor
University of Oxford · Other
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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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * 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 * Ability to understand the study instructions and provi…
Contacts

Cindy Chu, MD, PhD

+856 (0) 21 250 752

cindy@tropmedres.ac

CONTACT