Phase 2 Macular Degeneration Trial, Recruiting NCT07630649 Sponsor: Adverum Biotechnologies, Inc. Condition: Macular Degeneration
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Phase 2 Macular Degeneration Trial, Recruiting

NCT07630649
Recruiting Phase 2

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 50 years old or older at the time of your first screening visit
  • You are willing to use an acceptable form of birth control during the trial
  • You have been diagnosed with abnormal blood vessel growth behind both eyes (a condition called bilateral CNV) caused by wet age-related macular degeneration (wet AMD) in both eyes
  • Your vision (measured using a standard eye chart test) falls within a specific range required by the trial, depending on whether you have previously received the study treatment (Ixo-vec) or not (confirm with trial site for exact vision requirements)
  • You have a history of prior treatment with anti-VEGF injections (a common wet AMD treatment), and if applicable, prior exposure to the study treatment Ixo-vec, in line with the trial's requirements
  • Your eyes have shown a meaningful positive response to anti-VEGF injections, as defined by the trial (confirm with trial site)
  • You are able and willing to follow all study procedures as judged by the study doctor

Who may not be able to join:

  • You have a serious health condition, illness, or abnormal test result that could make the study treatment unsafe for you or make it hard to participate, including — in some cases — a history of severe COVID-19 (confirm with trial site)
  • You have previously received any gene therapy other than Ixo-vec (if Ixo-vec applies to you)
  • You are currently taking steroid medications that affect the relevant eye or eyes at the time of your first screening visit
  • You have received another investigational treatment or medical device in the relevant eye within the past 3 months
  • You have a known allergy or bad reaction to any of the products or ingredients used in this trial
  • You have poorly controlled diabetes or a blood sugar control measurement (HbA1c) of 8.0% or higher
  • You have a history of certain heart or blood vessel diseases, or ongoing bleeding disorders (confirm with trial site for specifics)
  • You have taken immune-suppressing medications within a certain period before the trial (confirm with trial site for exact timeframe)
  • You have received systemic (whole-body) anti-VEGF treatment within a certain period before the trial (confirm with trial site for exact timeframe)
  • You have been diagnosed with cancer within the past 5 years, unless it has been fully and adequately treated as defined by the trial
  • You have an active infection in or around the relevant eye or eyes
  • You have another eye condition in the relevant eye (beyond wet AMD) that could affect your vision, interfere with assessments, or require treatment during the trial
  • You have had certain prior eye surgeries or treatments that could affect the trial results or increase your risk (confirm with trial site for specifics)
  • You have a history of a detached retina or a tear in the layer beneath your retina in the relevant eye
  • You have uncontrolled high pressure in your eye or uncontrolled glaucoma, as defined by the trial
  • You have a history of significant inflammation inside the eye (specifically, inflammatory cells rated 2+ or higher) in certain eyes, which may increase the risk of eye inflammation (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 27 July 2026
Phase 2: approximately ~30% 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 2
Sponsor
Adverum Biotechnologies, Inc.
Registry
ClinicalTrials.gov
Start date
2 June 2026
Est. completion
1 June 2031

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of ocular adverse events (AEs); Incidence of ocular serious adverse events (SAEs).; Incidence of non-ocular serious adverse events (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: 27 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