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Clinical Trial Summary

Health care facility based, randomized, controlled, open label, superiority trial with 3 arms


Clinical Trial Description

- To assess the effectiveness of a short-course of high dose primaquine (total dose 7mg/kg given unsupervised over 7 days) compared to the current standard low dose primaquine regimen (total dose 3.5mg/kg given unsupervised over 14 days). - To assess the effectiveness of tafenoquine (single dose of 300mg) compared to the short-course high dose primaquine regimen. - To assess the safety of tafenoquine compared to the high and low dose primaquine regimens. - To assess the cost-effectiveness and feasibility of high dose primaquine and tafenoquine compared to the current low dose primaquine regimen ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04411836
Study type Interventional
Source Menzies School of Health Research
Contact Kamala Thriemer, MD, MPH, PhD
Phone 0889468644
Email kamala.ley-thriemer@menzies.edu.au
Status Recruiting
Phase Phase 3
Start date April 25, 2021
Completion date September 30, 2024

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