drugset / Trial / NCT07468513

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)

Timeline

Start
2024-05-17
Primary completion
2028-06-30
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Comparator Primaquine Small molecule 0.75 mg/kg
Comparator Primaquine Small molecule 1 mg/kg