NDAORALTABLET1 Generic Approved
Approved
May 2020
Lifecycle
Peak
Competitive Pressure
15/100
Clinical Trials
9
Data completeness
7/8 — Comprehensive
FERRIPROX (deferiprone) by Chiesi is iron chelating activity [moa]. Approved for iron chelator [epc]. First approved in 2020.
Drug data last refreshed 22h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
FERRIPROX (deferiprone) is an oral iron chelator approved by the FDA in May 2020 for treating iron overload in patients with chronic transfusion-dependent anemias. It works by binding excess iron and facilitating its urinary excretion, addressing a critical unmet need in transfusion-dependent populations. The tablet formulation offers a convenient alternative to intravenous chelation therapies.
$0.004BPart D
Peak12.5 years to LOEProduct is at peak lifecycle stage with modest Part D utilization (277 claims in 2023), suggesting niche positioning in a specialized patient population with limited near-term growth visibility.
Mechanism of Action
Iron Chelating Activity
Pharmacologic Class:
Iron Chelator
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (9)
Safety and Acceptability of Deferiprone Delayed Release Tablets in Patients With Systemic Iron Overload
Started Mar 2019
30 enrolled
Iron Overload Due to Repeated Red Blood Cell Transfusions
Safety and Efficacy of Early Treatment With Deferiprone in Infants and Young Children
Started Nov 2018
64 enrolled
Beta Thalassemia Major AnemiaIron Overload
Study of Parkinson's Early Stage With Deferiprone
Started Oct 2016
140 enrolled
Parkinson's Disease
Long-term Safety and Efficacy of Ferriprox® in Iron Overloaded Patients With Sickle Cell Disease or Other Anemias
Started May 2015
134 enrolled
Iron OverloadSickle Cell DiseaseOther Anemias
Long-term Deferiprone Treatment in Patients With Pantothenate Kinase-Associated Neurodegeneration
Started Jun 2014
68 enrolled
Pantothenate Kinase-Associated Neurodegeneration
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.