EarLy Treatment Response in nEoVascular Macular Degeneration With Eylea 8mg: ELEV8 A Prospective Observational Open Label Study Investigating the Fluid Dynamics During Early Response to Aflibercept 8mg in Patients With Exudative Age-related Macular Degeneration (AMD).
- Sponsor
- Insel Gruppe AG, University Hospital Bern
- Study ID
- NCT07434713
- Status
- Recruiting
Conditions
- Age-Related Macular Degeneration (AMD)
Eligibility Criteria
- Sex
- ALL
- Age
- 50 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- treatment with Aflibercept 8mg (Eylea) — DRUGintravitreal injection of 8mg aflibercept
Study Details
This prospective, observational, open-label study evaluates early treatment response to intravitreal aflibercept 8 mg in patients with exudative age-related macular degeneration. Retinal fluid dynamics assessed by optical coherence tomography and changes in best-corrected visual acuity two months after baseline are analyzed to characterize early treatment outcomes.
Key Dates
- Start date
- Jul 14, 2025
- Status verified
- Feb 2026
- Primary completion
- Mar 27, 2026
- Completion
- Mar 27, 2026
Study Design
- Enrollment
- 50 participants (estimated)
Arms
- Arm: all study participants
Primary Outcome Measure
Fluid dynamics on OCT scans during the early treatment phase of macular degeneration with Aflibercept 8mg. [ Time Frame: Each participant is followed up for 2 months after their treatment with aflibercept 8mg. From study enrollment and the 1st injection, over weekly check ups until the 2nd injection, completed with a last visit and the 3rd and last injection. ]
Central Contacts
- Florian M Heussen, Dr. med.+41 (0)31 664 54 24
- Martin S Zinkernagel, Prof. Dr. Dr. med.+41 (0)31 632 85 03
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