Deferiprone

(Ferriprox®)

Ferriprox®

Drug updated on 11/1/2024

Dosage FormTablet (oral; 500 mg, 1000 mg)
Drug ClassIron chelators
Ongoing and
Completed Studies
ClinicalTrials.gov

Indication

  • Indicated for the treatment of transfusional iron overload in adult and pediatric patients 8 years of age and older with thalassemia syndromes, sickle cell disease or other anemias.

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Summary
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  • This summary is based on the review of four systematic review(s)/meta-analysis(es). [1-4]
  • Iron Chelation Therapy (ICT) in Thalassemia Patients: Deferiprone showed high compliance rates (87.2-92.2%) compared to desferioxamine (48.84-85.1%) and deferasirox (90-100%). Increased compliance correlated with lower serum ferritin levels, reduced risks of liver and cardiac diseases, endocrinologic morbidity, and improved health-related quality of life (HRQoL).
  • Friedreich Ataxia (FA): Deferiprone showed no significant improvement across severity scales (ICARS, FARS, SARA, ADL), with most studies reporting patient deterioration regardless of intervention or inconclusive results.
  • Sickle Cell Disease (SCD) and Thalassemia: Adherence rates for deferiprone ranged from 69% to 95% compared to deferoxamine (71% to 93%), with trials reporting no difference in quality of life (QoL) outcomes.
  • Friedreich Ataxia (FA): Serious adverse events (SAEs) reported with deferiprone include atrial fibrillation, craniocerebral injury, and ventricular tachycardia.
  • Sickle Cell Disease (SCD), Thalassemia, and Superficial Siderosis: SAEs associated with deferiprone include a 1-2% risk of agranulocytosis in SCD and thalassemia, with superficial siderosis patients experiencing a 21.7% incidence of anemia, 8.7% incidence of neutropenia, and 5.8% incidence of agranulocytosis.
  • There is no population type or subgroup information available in the reviewed studies.