CompletedPhase 1NCT04002687
Determine the Tolerability and Safety of Atovaquone-proguanil (ATV-PG) Co-administered With Amodiaquine (AQ)
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
- Ulrike Lorch, MD FRCA FFPMRichmond Pharmacology Limited
- Intervention
- ATV-PG 1000-400 mg + AQ 612 mg(drug)
- Enrollment
- 44 target
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2019 – 2019
Study locations (1)
- Richmond Pharmacology Ltd., Croydon, London, United Kingdom
Collaborators
Richmond Pharmacology Limited
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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