Phase 3 Macular Degeneration Trial, Recruiting NCT07064759 Sponsor: 4D Molecular Therapeutics Condition: Macular Degeneration
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Phase 3 Macular Degeneration Trial, Recruiting

NCT07064759
Recruiting Phase 3 🇦🇺 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:

  • You are 50 years of age or older at the time you give consent
  • You have been diagnosed with a specific type of wet age-related macular degeneration (wet AMD) that has caused abnormal blood vessel growth in your eye, and you have either never received eye injections for this condition, or you have had no more than 4 eye injections and were diagnosed no more than 6 months before the screening visit
  • The abnormal blood vessels in your eye are currently active and causing fluid or leakage, as confirmed by eye imaging tests at your screening visit
  • Your eye has shown a positive response to a specific eye injection medication called aflibercept, as confirmed by an independent review center
  • Your vision in the study eye falls within a specific range — roughly between 20/320 and 20/32 on a standard eye chart — at the screening visit
  • The thickness of the central part of your retina is at or below a certain measurement (500 microns) at the screening visit, as confirmed by an independent review center

Who may not be able to join:

  • The abnormal blood vessel growth in your eye is caused by something other than wet AMD, or there is scarring, tissue loss, or significant bleeding in the central part of your retina
  • You have a history of a detached retina in the study eye
  • You have a history of or currently have active inflammation in either eye
  • You have glaucoma or high pressure in your eye that requires more than 2 eye drop medications to control
  • You have had any previous or ongoing treatments for the abnormal blood vessels or certain eye structure problems in the study eye, other than the allowed eye injections mentioned above
  • You have had a major illness or major surgery in the 28 days before your screening visit
  • You have uncontrolled high blood pressure
  • You have had a heart attack, certain heart procedures, stroke, or a mini-stroke within 6 months of the screening visit
  • You have a history of an autoimmune condition that could increase the risk of eye inflammation (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 26 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

Principal Investigator: Julie Tsai, MD, 4D Molecular Therapeutics

Phone: (888) 748-8881

Australian sites

Adelaide Eye and Retina Centre, Adelaide,
Eye Clinic Albury Wodonga, Albury,
Strathfield Retina Clinic, Strathfield,
Sydney Retina Clinic and Day Surgery, Sydney,

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
4D Molecular Therapeutics
Registry
ClinicalTrials.gov
Start date
22 July 2025
Est. completion
1 November 2028

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇧🇬 Bulgaria 🇩🇪 Germany 🇭🇺 Hungary 🇮🇹 Italy 🇯🇵 Japan 🇱🇻 Latvia 🇱🇹 Lithuania 🇵🇹 Portugal 🇸🇬 Singapore 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Mean change from baseline in Best Corrected Visual Accuity (BCVA) Early Treatment for Diabetic Retinopathy (ETDRS) letter score at Week 52

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: 26 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