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Drug

Deferiprone

Approved · EMA
Emerging researchLate-stage development
Also known as Ferriprox, Deferiprona, Défériprone, 1,2-Dimethyl-3-hydroxypyrid-4-one+2 more

Ferriprox, Deferiprona, Défériprone, 1,2-Dimethyl-3-hydroxypyrid-4-one, 3-Hydroxy-1,2-dimethyl-4(1H)-pyridone, Deferipronum.

1
Research papers
2
Active clinical trials
1
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Cardiac MRI-guided Deferiprone Therapy for Acute Myocardial Infarction Patients

Clinical trial2026-04-08Results expected Q1 2029 · ClinicalTrials.gov

Approval: Ferriprox (EMA)

Regulatory1999-08-25EMA

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Deferiprone
Aliases & brands
FerriproxDeferipronaDéfériprone1,2-Dimethyl-3-hydroxypyrid-4-one3-Hydroxy-1,2-dimethyl-4(1H)-pyridoneDeferipronum
RxNorm CUI
11645
ChEMBL ID
CHEMBL70927
ATC codes
V03AC02
UNII
2BTY8KH53L
Regulatory jurisdictions
ema

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
1999-08-25
Latest approval
1999-08-25
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
1999-08-25Approval
Approval: Ferriprox (EMA)
Indication: Ferriprox monotherapy is indicated for the treatment of iron overload in patients with thalassaemia major when current chelation therapy is contraindicated or inadequate.Show full indication

Ferriprox monotherapy is indicated for the treatment of iron overload in patients with thalassaemia major when current chelation therapy is contraindicated or inadequate. Ferriprox in combination with another chelator is indicated in patients with thalassaemia major when monotherapy with any iron chelator is ineffective, or when prevention or treatment of life-threatening consequences of iron overload (mainly cardiac overload) justifies rapid or intensive correction.

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

37 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
37
registered trials across all phases
LATEST COMPLETION 2024
2
Active studies
2
Recruiting
19
Late-stage (III+)
25
Completed
10
Discontinued
PHASE DISTRIBUTIONn = 37
Early Phase 11Phase 15Phase 1 / 21Phase 211Phase 2 / 34Phase 36Phase 48Phase N / A1

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

Research activity

1 papers

Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.

Major research themes3
Immunity, Innate1Iron Chelating Agents1Ovarian Neoplasms1
Journals, researchers & institutions
Top journals
  • Cancer discovery1
Leading researchers
  • Awasthi D1
  • Cantillo E1
  • Chae CS1
  • Chapman-Davis E1
  • Cloonan SM1
  • Cubillos-Ruiz JR1
  • Emmanuelli A1
  • Frey MK1
Leading institutions
free-text, unnormalised
  • Caryl and Israel Englander Institute for Precision Medicine1
  • Foundation for the Finnish Cancer Institute1
  • Sandra and Edward Meyer Cancer Center1
  • School of Medicine1
  • The HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine1
  • Tisch Cancer Institute1
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • Europe PMC — research literature
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.