Clinical Trial

First in Human Study of BETA-TT8 in wetAge-related Macular Degeneration (wetAMD)

Study acronym: BEyOND
Not Yet Recruiting Phase 1/2
View on ClinicalTrials.gov →
Summary
This is a first-in-human clinical trial evaluating the safety and tolerability of BETA-TT8 Ophthalmic Gel in people with wet age-related macular degeneration (AMD). Approximately 24 participants with stable wet AMD who have previously received at least three anti- Vascular Endothelial Growth Factor (anti -VEGF) injections will use the eye gel for up to 12 weeks at one of three dosing schedules (once, twice, or three times daily). Standard anti-VEGF treatment (aflibercept) will remain available if needed during the study. Participants who complete the initial 12-week treatment period may be invited to continue in an extension phase for up to 12 months to collect additional safety and treatment information.
Trial Details
NCT Number NCT07766473
Lead Sponsor Filamon LTD
Conditions Neovascular (Wet) Age-Related Macular Degeneration
Enrollment 24 participants
Start Date 2026-09
Primary Completion 2027-03 (estimated)
Study Completion 2027-09 (estimated)
Updated on ClinicalTrials.gov 2026-08-14