TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

EGATEN

TRICLABENDAZOLE Cytochrome P450 2C19 Inhibitors
Approved 2019-02-13
1
Indication
--
Phase 3 Trials
1
Priority Reviews
7
Years on Market

Details

Status
Prescription
First Approved
2019-02-13
Routes
ORAL
Dosage Forms
TABLET

Companies

Active Ingredient: TRICLABENDAZOLE

EGATEN Approval History

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What EGATEN Treats

1 indications

EGATEN is approved for 1 conditions since its original approval in 2019. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Fascioliasis
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.

EGATEN FDA Label Details

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Indications & Usage

FDA Label (PDF)

EGATEN ® is indicated for the treatment of fascioliasis in patients 6 years of age and older. EGATEN ® tablet is an anthelmintic indicated for the treatment of fascioliasis in patients 6 years of age and older.

EGATEN Patents & Exclusivity

Exclusivity: Feb 2026

Exclusivity

ODE-228 Until Feb 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.