Phase 1 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting NCT06701721 Sponsor: Therini Bio Pty Ltd Condition: Retinal Vein Occlusion and Diabetic Macular Oedema
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Phase 1 Retinal Vein Occlusion and Diabetic Macular Oedema Trial, Recruiting

NCT06701721
Recruiting Phase 1 🇦🇺 Australian site

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 understand the study procedures and risks, and can provide written consent before any study-related activities begin
  • People aged 18 to 80 years old (inclusive) at the time of giving consent
  • People who have been diagnosed with Diabetic Macular Edema (DME), a condition where fluid builds up in the central part of the retina due to diabetes
  • People who have experienced vision loss in the eye being studied

Who may not be able to join:

  • People who are pregnant or breastfeeding
  • People who have had cataract surgery or any other eye surgery on the study eye within the 3 months before the screening visit
  • People who have any other eye or health condition, aside from DME, that could affect how the study results are interpreted (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 27 July 2026
Phase 1: approximately ~10% 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: Joel Naor, Therini Bio, Inc.

Phone: +1 (925) 819-1952

Australian sites

Marsden Eye Specialists, Parramatta, New South Wales
+ 61 2 9635 7077
South Eastern Sydney Local Health District, Sydney, New South Wales
+61 02 9382 7309
Sydney West Retina, Westmead, New South Wales
+61 2 9893 9022
Princess Alexandria Hospital, Woolloongabba, Queensland
+61 7 3443 8050
Royal Adelaide Hospital, Adelaide, South Australia
+61 08 7074 2257
Sunshine Eye Surgeons, Albans, Victoria
+61 3 9077 3235
Eye Surgery Associates Pty Ltd, Malvern, Victoria
+61 402 133 315

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 1
Sponsor
Therini Bio Pty Ltd
Registry
ClinicalTrials.gov
Start date
20 December 2024
Est. completion
31 March 2027

Where this trial is recruiting

🇦🇺 Australia

7 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Adverse Events

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