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 who have signed a consent form before taking part in the research
- Men or women aged 50 or older at the time of signing the consent form
- People who have abnormal blood vessel growth (called CNV) under or involving the central area of the retina (the macula), caused by a condition known as wet age-related macular degeneration (wet AMD)
- People whose vision in the study eye falls within a specific range on a standardised eye chart test (between 19 and 78 ETDRS letters, inclusive) at the start of the trial
Who may not be able to join:
- People whose study eye has other eye conditions or health conditions that, in the investigator's judgement, could interfere with treatment results or make the results difficult to interpret
- People whose study eye has glaucoma that cannot be controlled
- People who have an active infection or inflammation in or around either eye
- People whose non-study eye has severe vision loss
- People whose study eye received an anti-VEGF injection (a type of eye treatment) within 90 days before the start of the trial
- People whose study eye received an anti-complement treatment within 90 days before the start of the trial
- People whose study eye has ever received the specific study drug (IBI302) at any point before the trial
- People with high blood pressure that cannot be controlled
- People whose blood sugar control measure (HbA1c) was above 10.0% within 28 days before the screening visit
- People who meet any other exclusion criteria set out in the trial protocol (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: 86 15821084695
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
Proportion of participants whose best corrected visual acuity (BCVA) of the study eye decreased by less than 15 letters from baseline as measured by the visual acuity chart in the early treatment diabetic retinopathy study (ETDRS) at week 52
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.