Phase 3 Macular Degeneration Trial, Recruiting NCT07482176 Sponsor: Adverum Biotechnologies, Inc. Condition: Macular Degeneration
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Phase 3 Macular Degeneration Trial, Recruiting

NCT07482176
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:

  • You are able and willing to give your consent to participate (or have a legal representative who can do this on your behalf), and you are able to follow the study schedule and requirements
  • You have been diagnosed with a specific type of abnormal blood vessel growth in the eye (called CNV) caused by wet age-related macular degeneration (wet AMD) in the eye being studied, and the condition was active at your first screening visit
  • You are at least 50 years old at the time of your first screening visit
  • Your vision in the study eye falls within a specific range — roughly between 20/200 and 20/32 on a standard eye chart (confirm with trial site if unsure where your vision falls)
  • Your eye showed a meaningful improvement in its structure when treated with anti-VEGF injections (a common wet AMD treatment) during the screening period
  • You are able to reliably use eye drops as required by the study

Who may not be able to join:

  • You have a medical condition that the doctor believes could make the study treatment unsafe for you, make it hard for you to take part, or affect the study results — this may include a history of severe COVID-19 if it is likely to cause complications
  • You have previously received any type of gene therapy
  • You have taken part in a clinical trial using an experimental medicine or medical device in your study eye within the past 3 months (or longer, depending on the medicine)
  • You are pregnant, breastfeeding, or planning to become pregnant or breastfeed in the future
  • You have had a heart attack in the 6 months before the start of the study
  • You have high blood pressure that is not well controlled (confirm specific numbers with trial site)
  • You have had a stroke in the 6 months before the start of the study
  • You have an ongoing bleeding disorder (note: taking aspirin or certain blood thinners is generally allowed)
  • You have been taking immune-suppressing medications within the past 90 days — though short courses of steroids by mouth, or steroid use through inhaler, joints, nose spray, or skin cream, may be allowed
  • You have poorly controlled diabetes, or your blood sugar levels (measured by a specific blood test called HbA1c) are too high during screening
  • You have an active eye or surrounding eye area infection in your study eye
  • You have had eye surgery (including laser or corrective surgery) in your study eye within the past 5 months, or have ever had certain specific eye surgeries such as a cornea transplant, removal of the gel inside the eye (vitrectomy), or certain laser or surgical treatments for macular degeneration
  • You have a history of a detached retina or a tear in a specific layer of your eye (the retinal pigment epithelium) in the study eye
  • You have uncontrolled pressure inside your eye (glaucoma) in the study eye, are using two or more eye drops to lower eye pressure, or have had certain glaucoma surgeries in the study eye
  • You have ever had increased eye pressure caused by steroid eye drops in either eye
  • You have a history of eye inflammation (uveitis) in either eye, beyond mild post-surgical swelling that went away
  • You have ever been treated with a specific type of medication called a complement inhibitor for a condition called geographic atrophy in your study eye
  • You have a known history of certain viral eye infections (such as herpes or cytomegalovirus affecting the eyes) in either eye

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 20 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: Adam Turpcu, PhD, Adverum Biotechnologies, Inc.

Phone: 650-656-9323

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
Adverum Biotechnologies, Inc.
Registry
ClinicalTrials.gov
Start date
16 March 2026
Est. completion
15 November 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Mean Change from Baseline in BCVA Based on an Average at Weeks 52 and 56

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: 20 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