TheraRadar
Data updated: May 26, 2026

ENZEEVU (aflibercept-abzv)

Ophthalmology Approved 2024-08-09
1
Indication
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2024-08-09
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: AFLIBERCEPT-ABZV

ENZEEVU Approval History

2025
2026
Original
New Indication
New Form
Label Update
3 FDA actions from 2024 to 2026
Feb 2026 SUPPL
Label · Labeling
Feb 2025 SUPPL
Update
Aug 2024 ORIGINAL
Update

What ENZEEVU Treats

1 FDA approvals

Originally approved for its first indication in 2024 .

  • Other (1)
Biosimilar for Eylea

ENZEEVU is a lower-cost alternative to Eylea with no clinically meaningful differences. Requires prescriber approval to substitute.

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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.

ENZEEVU FDA Label Details

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Data Sources

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