Phase 3 Macular Degeneration Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged between 50 and 89 years old
- People whose vision in the study eye falls within a specific range on a standard eye chart test (confirm with trial site for exact letter score details)
- People who have been diagnosed with a specific type of age-related macular degeneration (AMD) affecting the central part of the retina, and who have already received anti-VEGF injections (a common eye treatment for AMD) for it
- People whose study eye has already had cataract surgery at least 12 weeks before joining the trial, with the natural lens replaced by an artificial one
- People who have shown a meaningful improvement in response to their previous anti-VEGF eye injections
- People who are willing and able to sign a written consent form agreeing to take part
For the two-eye treatment part of the trial (if applicable):
- People whose vision in both eyes falls within a specific range on a standard eye chart test (confirm with trial site)
- People who have the same AMD-related condition in both eyes
- People who have had cataract surgery with an artificial lens in both eyes, at least 12 weeks before joining
- People who still have active disease in the relevant eye at the time of joining
Who may not be able to join:
- People whose eye condition causing abnormal blood vessel growth or retinal swelling is due to something other than AMD
- People who have significant scarring or tissue loss at the central part of the retina in the study eye
- People whose study eye has another condition that, in the doctor's opinion, would prevent vision from improving
- People who have severe glaucoma, or a history of a certain type of secondary glaucoma, in the study eye
- People who have had a heart attack, stroke, or mini-stroke within the past 6 months
- People who have had eye surgery in the study eye within 12 weeks before being enrolled in the trial
- People who have received certain types of injections into the study eye (such as steroid injections or experimental treatments) — other than standard AMD injections — within a specific timeframe before the trial (confirm with trial site for exact timing details)
- People who have previously received gene therapy treatment of any kind
For the two-eye treatment part of the trial (if applicable), most of the above exclusions apply to both eyes or the second eye, depending on participation type (confirm with trial site).
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 1-833-711-0349
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Mean change from baseline in Best Corrected Visual Acuity (BCVA); Bilateral Treatment Substudy: Incidence of ocular AEs and any SAEs
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.