drugset / Trial / NCT01825512

Efficacy/Safety Study of Deferiprone Compared to Deferasirox in Paediatric Patients

NCT01825512

RandomizedParallel-groupOpen-labelTreatment

Summary

Multicentre, randomised, open label, non-inferiority active-controlled trial to evaluate efficacy and safety of a 12-months treatment with deferiprone (DFP) at dose of 75-100 mg/kg/day versus deferasirox (DFX) at dose of 20-40 mg/kg/day in paediatric patients (1 month \< 18 years old) affected by hereditary haemoglobinopathies and requiring frequent transfusions and chelation.

Timeline

Start
2014-03-17
Primary completion
2017-09-21
Completion
2017-09-21

Drugs

EvaluationDrugModalityDoseRoute
Comparator Deferasirox Unknown 20 mg/kg Oral
Comparator Deferasirox Unknown 40 mg/kg Oral
Subject Deferiprone Small molecule 75 mg/kg Oral
Subject Deferiprone Small molecule 100 mg/kg Oral