Phase 2 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting NCT07205887 Sponsor: EyeBiotech Ltd. Condition: Retinal Vein Occlusion and Diabetic Macular Oedema
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Phase 2 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting

NCT07205887
Recruiting Phase 2

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:

General:

  • A person must be willing and able to understand the study procedures and risks, and sign a written consent form before any study activities begin

For people with a new diagnosis of wet age-related macular degeneration (wet AMD) who have not yet received treatment:

  • The person must be 50 years of age or older
  • There must be abnormal blood vessel growth under or near the centre of the retina (the macula), affecting vision
  • The wet AMD diagnosis must have been made within 21 days before the first study treatment day

For people with wet AMD who have already received some treatment but have not fully responded:

  • The person must be 50 years of age or older
  • There must be abnormal blood vessel growth under or near the centre of the retina, affecting vision
  • The wet AMD diagnosis must have been made within 90 days before a specific screening visit

For people with Branch Retinal Vein Occlusion (BRVO — a blockage in a small vein in the retina):

  • The person must have a confirmed BRVO diagnosis in the eye being studied
  • The vision loss in the study eye must be primarily caused by the BRVO
  • The person must not have received prior treatment, and must have fluid build-up in the centre of the retina diagnosed within 9 months of screening

Who may not be able to join:

General:

  • People who are pregnant or breastfeeding
  • People who have had cataract surgery or certain minimally invasive glaucoma surgery in the study eye within 90 days before screening
  • People who have had a specific type of laser eye procedure (YAG laser capsulotomy) in the study eye within 90 days before screening
  • People currently taking certain medications known to be harmful to the retina, such as hydroxychloroquine, pentosan polysulfate sodium, or amiodarone

For people with wet AMD:

  • People who have previously had thermal laser treatment directed at the centre of the retina in the study eye
  • People who have previously had photodynamic therapy using a drug called Visudyne in the study eye

For people with BRVO:

  • People whose retinal swelling is caused by something other than BRVO, such as diabetic eye disease or wet AMD
  • People who have abnormal blood vessel growth in the iris or drainage angle of the eye, or a related form of glaucoma, in the study eye

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Charles Miller, MD PhD, EyeBiotech Ltd.

Phone: 212-914-0127

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

Status
Recruiting
Phase
Phase 2
Sponsor
EyeBiotech Ltd.
Registry
ClinicalTrials.gov
Start date
12 September 2025
Est. completion
30 June 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Change from baseline in Best-Corrected Visual Acuity measured using the standardized Early Treatment of Diabetic Retinopathy Study (ETDRS) chart

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov