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RECRUITING
NCT07468513
PHASE4

Primaquine for Vivax Malaria in G6PD Intermediate and Deficient Cases.

Sponsor: Menzies School of Health Research

View on ClinicalTrials.gov

Summary

A non randomized observation study that is aiming to assess the safety and efficacy of high dose primaquine (1mg/kg per day over 7 days) among patients with intermediate (30-70%) G6PD activity and the safety and efficacy of weekly primaquine among patients who are g6Pd deficient (\<30% activity)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2024-05-17

Completion Date

2028-12-31

Last Updated

2026-03-12

Healthy Volunteers

No

Interventions

DRUG

Patients with G6PD enzyme activities between 30 and <70% of the AMM will be treated with schizontocidal treatment plus high dose primaquine 1mg/kg/day for 7 days

Primaquine 1mg/kg/day for 7 days

DRUG

Patients with G6PD enzyme activities <30% of the AMM will be treated with schizontocidal treatment plus 8 weekly primaquine (0.75mg/kg dose).

8 weekly Primaquine (0.75mg/kg dose).

Locations (4)

Dr Marcus Lacerda

Manaus, Brazil

Arba Minch General Hospital

Arba Minch, Ethiopia

Dr Moses Laman and Dr Brioni Moore

Alexishafen, Madang Province, Papua New Guinea

Papua New Guinea Institute of Medical Research

Port Moresby, Magang, Papua New Guinea