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 diagnosed with Neovascular Age-related Macular Degeneration (a type of eye condition where abnormal blood vessels grow under the retina).
- People who are willing to sign a consent form agreeing to take part in the study.
- People who have already tried at least two standard eye injection treatments (Ranibizumab, Aflibercept, or Faricimab) without sufficient success, and are currently receiving these injections every 8 weeks or more frequently.
- People who are able to complete a required "wash-out period" (a waiting period after stopping their current eye injection) before joining — the length of this waiting period depends on which medication they are currently receiving (ranging from approximately 4 to 8 weeks depending on the drug).
- People whose eye scans show abnormal blood vessel activity in or near the central area of the retina, with signs such as fluid or abnormal tissue.
- People whose vision in the study eye falls within a specific range — roughly equivalent to being able to read between the 20/32 and 20/320 lines on a standard eye chart.
- People whose vision loss in the study eye is considered to be mainly caused by their retinal condition.
- People whose eye scans show the presence of fluid or certain structural changes in the central area of the retina.
- People whose liver, kidney, and blood test results are within an acceptable range (based on tests done within 7 days of starting treatment).
Who may not be able to join:
- People who have scarring, fibrous tissue, tissue wasting, or tears in the central part of the retina in the study eye.
- People with glaucoma (high pressure in the eye) that is not well controlled, even with medication (confirm with trial site).
- People with a history of a particular type of eye inflammation called uveitis that has no known cause or is linked to an immune system condition, in the study eye.
- People with a high degree of short-sightedness (at least 8 diopters) in the study eye, measured before any corrective eye surgery.
- People who have an active infection or inflammation around or outside the eye in either eye at the time of their initial assessment.
- People with high blood pressure that is not well controlled (specifically, a top reading above 160 or a bottom reading above 95).
- People currently taking steroid tablets (above a certain dose) or other medications that suppress the immune system for an ongoing condition.
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
Principal Investigator: Prof Qi Zeng, Intra-IMMUSG Pte Ltd
Phone: +65 65869661
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
Safety: Adverse Events according to CTCAE; Recommended Phase 2 Dose (PR2D); Efficacy: Best Corrected Visual Acuity (BCVA) measured by ETDRS letter score; Efficacy: Subfield Retinal Thickness (CST) measured by Optical Coherence Tomography (OCT)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.