Phase 3 Macular Degeneration Trial, Recruiting NCT05407636 Sponsor: AbbVie Condition: Macular Degeneration
Back to Macular Degeneration

Phase 3 Macular Degeneration Trial, Recruiting

NCT05407636
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:

  • People aged between 50 and 89 years old
  • People whose vision in the study eye falls within a specific range on a standard eye chart test (confirm with trial site for exact letter score details)
  • People who have been diagnosed with a specific type of age-related macular degeneration (AMD) affecting the central part of the retina, and who have already received anti-VEGF injections (a common eye treatment for AMD) for it
  • People whose study eye has already had cataract surgery at least 12 weeks before joining the trial, with the natural lens replaced by an artificial one
  • People who have shown a meaningful improvement in response to their previous anti-VEGF eye injections
  • People who are willing and able to sign a written consent form agreeing to take part

For the two-eye treatment part of the trial (if applicable):

  • People whose vision in both eyes falls within a specific range on a standard eye chart test (confirm with trial site)
  • People who have the same AMD-related condition in both eyes
  • People who have had cataract surgery with an artificial lens in both eyes, at least 12 weeks before joining
  • People who still have active disease in the relevant eye at the time of joining

Who may not be able to join:

  • People whose eye condition causing abnormal blood vessel growth or retinal swelling is due to something other than AMD
  • People who have significant scarring or tissue loss at the central part of the retina in the study eye
  • People whose study eye has another condition that, in the doctor's opinion, would prevent vision from improving
  • People who have severe glaucoma, or a history of a certain type of secondary glaucoma, in the study eye
  • People who have had a heart attack, stroke, or mini-stroke within the past 6 months
  • People who have had eye surgery in the study eye within 12 weeks before being enrolled in the trial
  • People who have received certain types of injections into the study eye (such as steroid injections or experimental treatments) — other than standard AMD injections — within a specific timeframe before the trial (confirm with trial site for exact timing details)
  • People who have previously received gene therapy treatment of any kind

For the two-eye treatment part of the trial (if applicable), most of the above exclusions apply to both eyes or the second eye, depending on participation type (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 21 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

Phone: 1-833-711-0349

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
13 January 2022
Est. completion
1 October 2026

Where this trial is recruiting

🇨🇦 Canada 🇫🇷 France 🇩🇪 Germany 🇭🇺 Hungary 🇮🇹 Italy 🇯🇵 Japan Puerto Rico 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Mean change from baseline in Best Corrected Visual Acuity (BCVA); Bilateral Treatment Substudy: Incidence of ocular AEs and any SAEs

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: 21 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