Phase 2 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting NCT06962839 Sponsor: Boehringer Ingelheim Condition: Retinal Vein Occlusion and Diabetic Macular Oedema
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Phase 2 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting

NCT06962839
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:

  • People who are 18 years of age or older
  • People who have been diagnosed with type 1 or type 2 diabetes, with a blood sugar control measurement (HbA1c) below 12%, and whose diabetes medication has been stable for at least 30 days before the study starts, with no major medication changes planned
  • People who have a specific type of eye swelling related to diabetes (called centre-involved diabetic macular edema) confirmed by a specialised eye scan, with the swelling in the central part of the retina measuring at or above a certain thickness (320 µm) in the eye being studied
  • People whose vision in the study eye falls within a specific range — roughly between 20/320 and 20/32 on a standard eye chart — as measured at the screening visit
  • Additional inclusion criteria may apply (confirm with trial site)

Who may not be able to join:

  • People whose macular swelling in the study eye is caused by something other than diabetic macular edema
  • People who have advanced diabetic eye disease with abnormal new blood vessel growth in the study eye, including growth on the iris or in the front part of the eye
  • People who have received certain injections into the eye (anti-VEGF treatments) within the past 4 to 6 months (depending on the specific medication used), or who have had more than 4 of these injections in total in the study eye
  • People who have previously had laser treatment to the retina, surgery inside the eye, steroid injections in or around the eye within the past 12 months, certain slow-release steroid implants at any time, or steroid or anti-inflammatory eye drops within the past 30 days
  • People who have active eye inflammation, or a history of inflammation inside the eye within the past year
  • People who are missing the natural lens of the eye or the membrane that holds it in place (certain exceptions may apply — confirm with trial site)
  • Additional exclusion criteria may apply (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.

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 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

Phone: 1-800-243-0127

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
Registry
ClinicalTrials.gov
Start date
5 June 2025
Est. completion
1 September 2027

Where this trial is recruiting

🇨🇳 China 🇨🇿 Czechia 🇩🇪 Germany 🇭🇺 Hungary 🇯🇵 Japan 🇵🇱 Poland 🇸🇰 Slovakia 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Occurrence (yes/no) of a gain of ≥10 Early Treatment Diabetic Retinopathy Study (ETDRS) letters compared with baseline in the study eye at Week 48

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