RecruitingPhase 4NCT04704999
Southeast Asia Dose Optimization of Tafenoquine
Studying Malaria
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University of Oxford
- Principal Investigator
- Cindy Chu, MD, PhDLao-Oxford-Mahosot Hospital-Wellcome Research Unit
- Intervention
- Tafenoquine(drug)
- Enrollment
- 700 target
- Eligibility
- 2 years · All sexes
- Timeline
- 2024 – 2028
Study locations (5)
- Mahidol Oxford Tropical Medicine Research Unit (MORU), Cambodia, Siem Reap, Cambodia
- Lao Oxford Mahosot Hospital Wellcome Trust Research Unit (LOMWRU), Vientiane, Laos
- Mahidol Vivax Research Unit (MVRU), Bangkok, Thailand
- Shoklo Malaria Research Unit (SMRU), Bangkok, Thailand
- Oxford University Clinical Research Unit (OUCRU), Bình Phước, Vietnam
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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