TheraRadar

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Data updated: Mar 10, 2026

DEFEROXAMINE MESYLATE

DEFEROXAMINE MESYLATE
Hematology Approved 2004-03-17
5
Indications
--
Phase 3 Trials
21
Years on Market

Details

Status
Prescription
First Approved
2004-03-17
Routes
INJECTION
Dosage Forms
INJECTABLE

DEFEROXAMINE MESYLATE Approval History

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What DEFEROXAMINE MESYLATE Treats

3 indications

DEFEROXAMINE MESYLATE is approved for 3 conditions since its original approval in 2004. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Iron Intoxication
  • Iron Overload
  • Chronic Anemia
Source: FDA Label
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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

DEFEROXAMINE MESYLATE FDA Label Details

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Indications & Usage

Deferoxamine mesylate for injection is an iron-chelating agent indicated: • As an adjunct to standard measures for the treatment of acute iron intoxication. • For the treatment of transfusional iron overload in patients with chronic anemia. Limitations of Use Deferoxamine mesylate for injection is not indicated for the treatment of primary hemochromatosis (since phlebotomy is the method of choice for removing excess iron in this disorder). 1.1 Acute Iron Intoxication Deferoxamine mesylate for injection is indicated as an adjunct to standard measures for the treatment of acute iron intoxication...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.