TheraRadar
Data updated: Mar 29, 2026

EYDENZELT

AFLIBERCEPT-BOAV
Approved 2025-10-02
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-10-02
Routes
INJECTION
Dosage Forms
INJECTABLE

Companies

Active Ingredient: AFLIBERCEPT-BOAV

EYDENZELT Approval History

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What EYDENZELT Treats

5 indications

EYDENZELT is approved for 5 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Neovascular Age-Related Macular Degeneration
  • Macular Edema
  • Retinal Vein Occlusion
  • Diabetic Macular Edema
  • Diabetic Retinopathy
Source: FDA Label

EYDENZELT Competitors

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4 other drugs also target PlGF. Compare mechanisms, indications, and trial activity.

Drug = Competitor name Company = Manufacturer N indic. = FDA-approved indications โ†’ Date = Patent/exclusivity expiry

Competitors share the same molecular target (PlGF). Earlier expiry dates signal biosimilar/generic opportunities.

Drugs Similar to EYDENZELT

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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.

EYDENZELT FDA Label Details

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Data Sources

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