Macular Degeneration Trial, Recruiting NCT06271330 Sponsor: Nantes University Hospital Condition: Macular Degeneration
Back to Macular Degeneration

Macular Degeneration Trial, Recruiting

NCT06271330
Recruiting Not Applicable

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 18 years old or older, male or female, and have been diagnosed with the "wet" (exudative) form of age-related macular degeneration (AMD).
  • You have been receiving eye injections of either ranibizumab or aflibercept for more than 1 year to treat your condition.
  • Your eye injections are currently needed more frequently than every 12 weeks (i.e., your injection intervals are shorter than 12 weeks).

Who may not be able to join:

  • You have severe short-sightedness, defined as having an eye length greater than 26 mm or a glasses prescription lower than -6 dioptres.
  • You have a condition called angioid streaks (crack-like lines in the back of the eye).
  • You have moderate or severe diabetic retinopathy (eye damage caused by diabetes).
  • You have a history of diabetic macular oedema (fluid build-up in the eye related to diabetes).
  • You have a history of uveitis (inflammation inside the eye).
  • You have previously had a retinal vein occlusion (a blockage of a blood vessel in the back of the eye).
  • You have a history of a condition called pseudovitelliform macular dystrophy (a rare inherited eye disorder — confirm with trial site if unsure).
  • You are currently under legal guardianship or trusteeship.
  • You are pregnant or currently breastfeeding.

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 14 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Jean-Baptiste Ducloyer, M.D, Nantes University Hospital

Phone: 02 40 08 34 01

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 April 2024
Est. completion
1 April 2025

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Difference in number of weeks between previous treatment (ranibizumab or aflibercept) and after 6 months of Faricimab treatment.

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: 14 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