Macular Degeneration Trial, Recruiting NCT06779773 Sponsor: Astellas Pharma Global Development, Inc. Condition: Macular Degeneration
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Macular Degeneration Trial, Recruiting

NCT06779773
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 have a condition called geographic atrophy (a type of damage to the center of the eye) caused by age-related macular degeneration (AMD), in one or both eyes
  • Your doctor has already decided that you should be treated with a medication called avacincaptad pegol (ACP), given as an injection into the eye
  • You are willing to fill out questionnaires about how your condition affects your daily life

Who may not be able to join:

  • You have an active infection in or around either eye
  • You have active inflammation (swelling or irritation) inside either eye
  • You have had an allergic reaction to avacincaptad pegol (ACP) or any of its ingredients
  • You are currently taking part in another research study that involves treatments outside of normal medical care
  • You have already received ACP injections in the eye that would be treated in this trial (note: if your other eye has received or is receiving ACP, you may still be eligible — confirm with trial site)
  • You have received a different type of eye injection called a complement inhibitor in either eye, unless it has been at least 90 days since your last dose of that medication (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 28 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: Medical Director, Astellas Pharma Global Development, Inc.

Phone: 800-555-5555

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
Sponsor
Astellas Pharma Global Development, Inc.
Registry
ClinicalTrials.gov
Start date
22 January 2025
Est. completion
31 October 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of ACP injections; Duration of treatment; Annual frequency of ACP injection; Reasons for discontinuation of treatment with ACP; Duration of the treatment interval; Site characteristics; Characteristics of patients with geographic atrophy (GA) secondary to AMD beginning treatment with Izervay

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: 28 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