TheraRadar

EyeBiotech

Pre-Approval PRO BETA
7
Total Trials
4
Phase 3
7
Phase 2
5
Recruiting
137
Score

Pipeline by Phase

Phase 3
4
Phase 2
7
Phase 1
2

Therapeutic Focus

Diabetic Macular Edema (DME) Macular Degeneration Age-Related Macular Degeneration Choroidal Neovascularization Wet Macular Degeneration

Clinical Trials (7)

NCT07440225 Phase 2 RECRUITING

A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)

Started: 3/27/2026

NCT07205887 Phase 2 RECRUITING

A Dose-masked Study of Intravitreal EYE103 in Participants With NVAMD or Macular Edema Following BRVO

Started: 9/12/2025

NCT07496567 Phase 2 NOT YET RECRUITING

A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-003)

Started: 4/30/2026

NCT06957080 Phase 2 ACTIVE NOT RECRUITING

A Study of 2 Doses of EYE103 Compared With Ranibizumab (0.5 mg) in Participants With DME

Started: 4/16/2025

NCT06571045 Phase 2 ACTIVE NOT RECRUITING

A Study to Evaluate the Efficacy and Safety of 2 Doses of EYE103 Compared With Ranibizumab (0.5 mg) in Participants With DME

Started: 8/7/2024

NCT06664502 Phase 1 ACTIVE NOT RECRUITING

A 2-part Study Consisting of a Multiple Ascending Dose Safety Study in Participants With Macular Edema Following Branch Retinal Vein Occlusion and a Dose-finding Safety and Preliminary Efficacy Study in Participants With Either Diabetic Macular Edema or Neovascular Age-related Macular Degeneration

Started: 11/12/2024

NCT05919693 Phase 1 COMPLETED

A 2-part Study Consisting of Multiple Ascending Dose (MAD) Safety Study, and a Dose-finding Masked Study to Assess the Safety and Efficacy of Intravitreal (IVT) EYE103 in Patients With Diabetic Macular Edema (DME) or Neovascular Age-related Macular Degeneration (NVAMD)

Started: 6/12/2023

Drug Candidates

Tiespectus Aflibercept EYE201 EYE103 Ranibizumab Aflibercept 2.0 mg
Activity Status: Active
Last Trial Started: 4/30/2026
Last Trial Ended: 8/26/2024
Trials (12 months): 3
Completed Trials: 1
Data sourced from ClinicalTrials.gov. This company has no FDA-approved drugs.