Phase 2 Macular Degeneration Trial, Recruiting NCT07668804 Sponsor: Theratocular Biotek Co. Condition: Macular Degeneration
Back to Macular Degeneration

Phase 2 Macular Degeneration Trial, Recruiting

NCT07668804
Recruiting Phase 2 🇦🇺 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:

  • Adults aged 50 or older who are able to give their agreement to participate and follow the study's requirements
  • People who have a specific type of vision loss called geographic atrophy (GA) caused by dry age-related macular degeneration (AMD), where the damaged area does not affect the central part of the retina — this must be confirmed by a specialist reading centre
  • People whose area of retinal damage falls within a specific size range, measured using a special eye imaging technique (confirm with trial site for exact details)
  • People who still have a minimum level of vision in the eye being studied — roughly the ability to read the top few lines of a standard eye chart
  • People whose eye pressure in the study eye is within a normal range

Who may not be able to join:

  • People who have recently taken part in certain other eye treatment studies or trials
  • Women who are pregnant or currently breastfeeding
  • People with a high degree of short-sightedness or an eye that is longer than a certain measurement
  • People who have previously received treatment for AMD, or who have a related condition involving abnormal blood vessel growth in the study eye
  • People who have had or currently have a condition involving inflammation inside the eye called uveitis
  • People who have recently received a specific type of medication that targets the complement system (part of the immune system)
  • People currently using certain medications that are not permitted in this trial, including experimental treatments or therapies that suppress the immune system

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 22 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: Dr. Andrew Chang, Sydney Retina Clinic & Day Surgery

Phone: +886 (2) 2790-6566

Australian sites

Retina & Eye Consultants, Hurstville, New South Wales (nsw)
+61 2 9570 1622
Sydney Retina Clinic & Day Surgery, Sydney, New South Wales (nsw)
+61 2 9221 3755
Launceston Eye Doctors, Launceston, Tasmania (tas)
+61 3 6334 0000

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
Theratocular Biotek Co.
Registry
ClinicalTrials.gov
Start date
2 June 2026
Est. completion
31 August 2027

Where this trial is recruiting

🇦🇺 Australia

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

Primary endpoints

Number of Participants with Treatment-Emergent Adverse Events (TEAEs)

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: 22 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