TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

HALAVEN

ERIBULIN MESYLATE
Oncology Approved 2010-11-15
3
Indications
--
Phase 3 Trials
3
Priority Reviews
15
Years on Market

Details

Status
Prescription
First Approved
2010-11-15
Routes
INTRAVENOUS
Dosage Forms
SOLUTION

Companies

Active Ingredient: ERIBULIN MESYLATE

HALAVEN Approval History

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What HALAVEN Treats

2 indications

HALAVEN is approved for 2 conditions since its original approval in 2010. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Metastatic Breast Cancer
  • Liposarcoma
Source: FDA Label
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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.

HALAVEN FDA Label Details

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Indications & Usage

FDA Label (PDF)

HALAVEN is a microtubule inhibitor indicated for the treatment of patients with: Metastatic breast cancer who have previously received at least two chemotherapeutic regimens for the treatment of metastatic disease. Prior therapy should have included an anthracycline and a taxane in either the adjuvant or metastatic setting. Unresectable or metastatic liposarcoma who have received a prior anthracycline-containing regimen. 1.1 Me tastatic Breast Cancer HALAVEN is indicated for the treatment of patients with metastatic breast cancer who have previously received at least two chemotherapeutic regim...

HALAVEN Patents & Exclusivity

Latest Patent: Jul 2027
Exclusivity: Mar 2026

Patents (2 active)

USRE46965*PED Expires Jul 8, 2027
USRE46965 Expires Jan 8, 2027

Exclusivity

M-280 Until Sep 2025
PED Until Mar 2026
Source: FDA Orange Book

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Data Sources

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