Phase 3 Macular Degeneration Trial, Recruiting NCT07007065 Sponsor: AbbVie Condition: Macular Degeneration
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Phase 3 Macular Degeneration Trial, Recruiting

NCT07007065
Recruiting Phase 3

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:

  • Your eye had cataract surgery at least 12 weeks before the first screening visit, and you now have an artificial lens in it.
  • You have been diagnosed with abnormal blood vessel growth (called choroidal neovascularization) in your eye caused by age-related macular degeneration (AMD), and the affected area is below a certain size (confirm with trial site).
  • You have received at least 2 injections into the eye (anti-VEGF treatment) in the past 6 months, and your doctor considers that your eye has responded to those injections.

Who may not be able to join:

  • The abnormal blood vessel growth or swelling in your eye is caused by something other than age-related macular degeneration.
  • You were diagnosed with the wet form of AMD more than 4 years before the first screening visit.
  • There is a certain type of fluid-filled blister (pigment epithelial detachment) in your eye that is larger than specific size limits, as measured by a specialist reading centre (confirm with trial site).
  • There is bleeding under the retina in your eye that covers more than half of the affected area, or that is located in the central part of your vision, as determined by a specialist reading centre.
  • There is a tear in a specific layer at the back of your eye (the retinal pigment epithelium) in the central part of your vision, as determined by a specialist reading centre.

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 23 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: ABBVIE INC., AbbVie

Phone: 844-663-3742

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
Registry
ClinicalTrials.gov
Start date
5 November 2025
Est. completion
1 March 2033

Where this trial is recruiting

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇦 Canada 🇭🇷 Croatia 🇨🇿 Czechia 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece 🇭🇺 Hungary 🇮🇱 Israel 🇮🇹 Italy 🇵🇹 Portugal Puerto Rico 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Annualized intravitreal anti-VEGF injection rate; Number of Participants Experiencing 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: 23 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