Phase 2 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting NCT06492876 Sponsor: Frontera Therapeutics Condition: Retinal Vein Occlusion and Diabetic Macular Oedema
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Phase 2 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting

NCT06492876
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 willing and able to follow the study procedures throughout the trial
  • People aged 18 to 74 years old at the time of signing the consent form
  • People who have been clinically diagnosed with centre-involving diabetic macular oedema (a specific type of swelling in the central part of the retina related to diabetes)
  • People whose best corrected vision score (measured using a standard eye chart with glasses or contact lenses if needed) in the eye being studied falls between 24 and 73 letters

Who may not be able to join:

  • People who have any other eye conditions in the studied eye — apart from diabetic macular oedema — that the investigator believes could affect vision improvement or would need treatment during the study to prevent or treat vision loss

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

Principal Investigator: Xiaorong Li, Professor, Tianjin Medical University Eye Hospital

Phone: +86-021-58206061

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
Frontera Therapeutics
Registry
ClinicalTrials.gov
Start date
15 November 2023
Est. completion
15 November 2024

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Safety and tolerability after FT-003 injection

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