Phase 2 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 16 years or older, of any gender
- People who are able to attend all scheduled visits and complete all required study assessments
- People who have been diagnosed with Stargardt Disease, confirmed through genetic testing
- People whose vision (with best possible correction) in both eyes meets the specific levels required by the study
- People whose eye scans show that certain layers of cells at the back of the eye are still present, as confirmed by a specialist imaging centre
- People who are in generally good health with adequately functioning organs
Who may not be able to join:
- People who have taken part in a clinical trial involving an experimental drug, agent, or therapy (for the eyes or otherwise) within the past six months
- People currently enrolled in another interventional clinical eye study
- People who have previously received any form of gene therapy (for the eyes or elsewhere), a retinal implant, or a cell-based eye treatment
- People who have pre-existing eye conditions in either eye that could interfere with the planned treatment or make it harder to interpret study results
- People who are known to respond to steroid medications by developing increased eye pressure that cannot be adequately managed with eye-drop pressure-lowering medications
- People with certain serious systemic (whole-body) illnesses where the disease itself, or its treatment, could affect eye or brain function — for example, those who have received radiation treatment near the eye area, or have a blood cancer affecting the optic nerve
- People with immune system problems, including conditions that weaken the immune system or those currently taking medications that suppress the immune system
- People who have had cataract surgery, other eye or refractive surgery, or injections in or around either eye within the four months before the screening visit
- People who have previously had a vitrectomy (a type of eye surgery) or who are missing the natural lens in the eye being studied
- People with a known sensitivity or allergy to any component of the study treatment, or to any medications planned for use around the time of the procedure (for example, povidone-iodine)
- People who have a known reason they cannot take the steroid preventive medication required by the study
- People who are currently pregnant or breastfeeding
- People with any other condition that would prevent them from completing all follow-up visits during the study
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: 858-617-8610
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
Incidence of Treatment-Emergent Adverse Events
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.