Last Updated: 31/10/2025

Safety, tolerability and pilot efficacy of short course, high dose primaquine treatment for liver stages of Plasmodium vivax infection

Objectives

The primary objective of this project is to assess the safety and tolerability of short course, high dose primaquine treatment in children.

Secondary objectives:

  • assess the pharmacokinetics of primaquine in children after high oral doses;
  • determine the efficacy of short course high dose primaquine compared to the standard 14 day treatment.

* Clinical Trial title: Investigation of Short Course, High Dose Primaquine Treatment for Liver Stages of Plasmodium Vivax Infection

Principal Investigators / Focal Persons

Brioni Moore

Study Design

ClinicalTrials.gov ID: NCT02364583

Study Type: Interventional
Study Phase: Phase 4
Study Design: 
Allocation: Non-Randomized
Interventional Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Date

Jun 2010 — Dec 2018

Country / Project Site(s)

Papua New Guinea

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