CompletedPhase 1NCT04456634
Assess Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Profile of Ruxolitinib With Artemether-lumefantrine
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
- Medicines for Malaria Venture
- Principal Investigator
- Paul Griffin, MDNucleus Network Corporate
- Intervention
- 20 mg/120 mg artemether-lumefantrine (AL) + 20 mg ruxolitinib phosphate (Rux)(drug)
- Enrollment
- 8 target
- Eligibility
- 18-55 years · All sexes
- Timeline
- 2020 – 2020
Study locations (1)
- Nucleus Network Brisbane, Brisbane, Queensland, Australia
Collaborators
Southern Star Research · Nucleus Network Ltd
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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