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NCT03748784 · ClinicalTrials.gov registry record · Phase 1

ADVM-022 Intravitreal Gene Therapy for Wet AMD

A Phase 1 study, sponsored by Adverum Biotechnologies.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target

NCT03748784: Completed Phase 1 study, sponsored by Adverum Biotechnologies.

NCT03748784 is a Phase 1 study that has completed, run by Adverum Biotechnologies. The registered enrollment target is 30 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03748784, a Phase 1 study, has completed, sponsored by Adverum Biotechnologies.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target

Study Summary

ADVM-022 (AAV.7m8-aflibercept) is a gene therapy product developed for the treatment of neovascular (wet) age-related macular degeneration (wet AMD). Wet AMD is a serious condition and the leading cause of blindness in the elderly. The available therapies for treating wet AMD require life-long intravitreal (IVT) injections every 4-12 weeks to maintain efficacy. A one-time IVT administration of ADVM-022 has the potential to treat wet AMD by providing durable expression of therapeutic levels of intraocular anti-VEGF protein (aflibercept) and maintaining the vision of patients. ADVM-022 is designed to reduce the current treatment burden which often results in undertreatment and vision loss in patients with wet AMD receiving anti-VEGF therapy in clinical practice.

Primary Outcome

Type, severity, and incidence of ocular and systemic adverse events (AEs)

Interventions

  • BIOLOGICAL ADVM-022

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2018-11-14
Est. Completion 2022-06-22
Phase Phase 1
Adverum Biotechnologies

10 total trials

What the finished NCT03748784 record still lists

NCT03748784 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (50% lower).

The record links to 0 conditions, and to 1 intervention - of which ADVM-022 is the first listed.

NCT03748784 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03748784 about?

NCT03748784 is a clinical study titled "ADVM-022 Intravitreal Gene Therapy for Wet AMD". ADVM-022 (AAV.7m8-aflibercept) is a gene therapy product developed for the treatment of neovascular (wet) age-related macular degeneration (wet AMD). Wet AMD is a serious condition and the leading cause of blindness in the elderly. The available therapies for treating wet AMD require life-long intra...

What is the current status of trial NCT03748784?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2018-11-14. Estimated completion is 2022-06-22.

What interventions are being tested in trial NCT03748784?

The interventions under investigation include: ADVM-022 (BIOLOGICAL).

Who is sponsoring clinical trial NCT03748784?

This trial is sponsored by Adverum Biotechnologies, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03748784's enrollment target sits among peer trials

30 1332nd of 2000 higher than 561 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03748784, the US trial registry maintained by the National Library of Medicine. NCT03748784 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.