The purpose of this study is to determine the safety and efficacy of an ocular sirolimus (rapamycin) formulation via different injection routes in patients with treatment-naive sub-foveal choroidal neovascularization secondary to age-related macular degeneration.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
20
Retinal Consultants of Arizona
Phoenix, Arizona, United States
Best-corrected visual acuity by ETDRS
Time frame: 180 days
Best-corrected visual acuity by ETDRS
Time frame: 60 days, 120 days
Safety across injection routes
Time frame: Through 1 year
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.