TheraRadar
Data updated: May 26, 2026

MYOVIEW (technetium tc-99m tetrofosmin kit)

Cardiovascular Approved 1996-02-09

Myoview is a radioactive diagnostic agent indicated for myocardial perfusion imaging (MPI) under both rest and stress (exercise or pharmacologic) conditions. It is used to delineate regions of reversible myocardial ischemia or infarcted myocardium in patients with known or suspected coronary artery disease. Additionally, Myoview is indicated for the assessment of left ventricular function, specifically left ventricular ejection fraction (LVEF) and wall motion, in patients with known or suspected heart disease.

Source: FDA Label • MEDI-PHYSICS

How MYOVIEW Works

Technetium (99mTc) tetrofosmin is a lipophilic, cationic complex that diffuses passively across cell membranes. It is actively retained within myocardial cells that possess intact mitochondria, serving as a marker for cell viability. Following intravenous injection, the agent is distributed within the myocardium in proportion to regional myocardial perfusion and the presence of viable tissue.

3
Indications
--
Phase 3 Trials
30
Years on Market

Details

Status
Prescription
First Approved
1996-02-09
Patent Cliff
2030

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Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

MYOVIEW Approval History

1997
1998
1999
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2003
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Original
New Indication
New Form
Label Update
21 FDA actions from 1996 to 2022 · 2 indication expansions
Dec 2022 SUPPL
Label · Labeling
Mar 2022 SUPPL
Label · Labeling
Apr 2017 SUPPL
Label · Labeling

What MYOVIEW Treats

4 indications

MYOVIEW is approved for 4 conditions since its original approval in 1996. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Myocardial Ischemia
  • Myocardial Infarction
  • Coronary Artery Disease
  • Heart Disease
Source: FDA Label

MYOVIEW Competitive Set

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Three rings of competition based on shared molecular targets and treated indications.

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

Drugs Similar to MYOVIEW

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Active Pipeline

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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.

MYOVIEW FDA Label Details

Indications & Usage

FDA Label (PDF)

MYOVIEW is indicated for the treatment of Myocardial Ischemia; Myocardial Infarction; Coronary Artery Disease; Heart Disease.

View full patent landscape →
1 OB patents · 1 families · 13 international docs across 8 countries

MYOVIEW Patents & Exclusivity

Latest Patent: Mar 2030

Patents (1 active)

US9549999 Expires Mar 10, 2030
Source: FDA Orange Book

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Deep insights for MYOVIEW

Revenue Insights

  • Quarterly revenue tracking
  • Historical trend analysis

Patent Timeline

  • Cliff: 2030
  • 1 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 20 similar drugs
  • Same target/indication analysis
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Data Sources

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