Phase 3 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting NCT07449936 Sponsor: EyePoint Pharmaceuticals, Inc. Condition: Retinal Vein Occlusion and Diabetic Macular Oedema
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Phase 3 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting

NCT07449936
Recruiting Phase 3

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 been diagnosed with fluid build-up in the central part of the eye (called macular edema) linked to diabetes-related eye disease, whether or not they have had previous treatment for this condition.
  • People whose vision in the eye being studied falls within a specific range — not too severely impaired and not near-perfect — as measured by a standard eye chart test at two separate appointments before the trial begins.
  • People who have had previous treatment must have received at least one injection of a specific type of eye medication (called anti-VEGF) in the past 12 months, and their most recent injection must have been given at least 12 weeks before the initial screening appointment.

Who may not be able to join:

  • People whose vision in the eye that is not being studied has fallen below a certain level of severity on a standard eye chart test (confirm with trial site for exact measurements).

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 28 July 2026
Phase 3: approximately ~65% 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

Phone: 833-393-7646

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 3
Sponsor
EyePoint Pharmaceuticals, Inc.
Registry
ClinicalTrials.gov
Start date
16 February 2026
Est. completion
1 October 2027

Where this trial is recruiting

🇩🇪 Germany 🇮🇱 Israel 🇵🇱 Poland 🇸🇰 Slovakia 🇺🇸 United States

Primary endpoints

Average change in best corrected visual acuity (BCVA)

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: 28 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