A Phase 1/2a 2-part Study Consisting of an Open-label Multiple Ascending Dose (MAD) Safety Study in Participants With Macular Edema Following Branch Retinal Vein Occlusion (BRVO), and a Dose-finding, Double-masked, Comparative Safety, and Preliminary Efficacy Study of Intravitreal (IVT) EYE201 (Tiespectus) in Participants With Either Diabetic Macular Edema (DME) or Neovascular Age-related Macular Degeneration (NVAMD)
Latest Information Update: 24 Mar 2026
At a glance
- Drugs EYE 201 (Primary)
- Indications Age-related macular degeneration; Branch retinal vein occlusion; Diabetic macular oedema; Retinal oedema; Wet age-related macular degeneration
- Focus Adverse reactions
- Sponsors Merck & Co
Most Recent Events
- 18 Mar 2026 Planned End Date changed from 1 May 2026 to 31 May 2026.
- 18 Mar 2026 Planned primary completion date changed from 1 Apr 2026 to 30 Apr 2026.
- 18 Mar 2026 Status changed from recruiting to active, no longer recruiting.