TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

XOFIGO

RADIUM RA-223 DICHLORIDE
Oncology Approved 2013-05-15
1
Indication
--
Phase 3 Trials
1
Priority Reviews
12
Years on Market

Details

Status
Prescription
First Approved
2013-05-15
Routes
INTRAVENOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: RADIUM RA-223 DICHLORIDE

XOFIGO Approval History

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What XOFIGO Treats

2 indications

XOFIGO is approved for 2 conditions since its original approval in 2013. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Castration-Resistant Prostate Cancer
  • Bone Metastases
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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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.

XOFIGO FDA Label Details

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Indications & Usage

FDA Label (PDF)

Xofigo is indicated for the treatment of patients with castration-resistant prostate cancer, symptomatic bone metastases and no known visceral metastatic disease. Xofigo is an alpha particle-emitting radioactive therapeutic agent indicated for the treatment of patients with castration-resistant prostate cancer, symptomatic bone metastases and no known visceral metastatic disease.

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Data Sources

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