drugset / Trial / NCT05637255

A Randomized, Double Masked, Parallel Group, Dose-finding Study to Evaluate SYL1801 in Patients With Neovascular Age-related Macular Degeneration (AMD)

NCT05637255 ↗

Phase 2 Completed 99 enrolled Sylentis, S.A.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The goal of this clinical trial is to compare the safety and effect on visual acuity of three different doses of SYL1801 eye drops.

Timeline

Start
2022-11-22
Primary completion
2024-12-19
Completion
2024-12-19

Outcome

Met primary endpoint

release “The middle concentration of 25mg/ml achieved a statistically significant improvement of visual acuity at 42 days (p=0.045).” pharmamar.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject SYL1801 Unknown — Other