UpcomingInterventionalPhase 1

A Clinical Study of Piperaquine, Pyronaridine, and Artesunate Administered in Combination in Healthy Adults

A Randomized, Open-Label Crossover Study to Evaluate Potential Pharmacokinetic Interactions of Orally Administered Piperaquine, Pyronaridine and Artesunate in Healthy Adult Participants

This is a registered study tracked in the Sterling IMRES research watch. It is sponsored by University of Oxford and run by the investigators named in the registry, not by Sterling IMRES. Details come from ClinicalTrials.gov, last updated 5 August 2026.

Summary

This University of Oxford Phase 1 study in Thailand will give healthy adult volunteers three regimens in randomised sequence: piperaquine alone, pyronaridine-artesunate alone, and all three drugs together. Each course runs for three days with follow-up and washout periods between regimens. The aim is to understand how the drugs interact before wider use of triple artemisinin-based combinations.

Objectives

  • Assess the safety of combining piperaquine with pyronaridine-artesunate in healthy adults.
  • Characterise the pharmacokinetics of each drug alone and in a triple combination.

Methodology

Study design
Randomized, crossover assignment, open label, primary purpose: health services research
Conditions
Malaria
Interventions
Piperaquine (drug); Artesunate-pyronaridine (Pyramax) (drug); Piperaquine and artesunate-pyronaridine (Pyramax) (drug)
Primary outcome
Number of adverse events
Sample size
24 participants (estimated)
Locations
Thailand
0

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