Efficacy and Safety Study of Ixoberogene Soroparvovec (Ixo-vec) in Participants With Neovascular Age-related Macular Degeneration (AQUARIUS)

Summary

This is a multi-center, randomized, double-masked, active-comparator-controlled, Phase 3 study in a broad participant population (treatment-naïve and treatment-experienced) with neovascular (wet) age-related macular degeneration (nAMD). The study will evaluate a single intravitreal (IVT) injection of Ixo-vec compared to intravitreal aflibercept (active comparator). The primary endpoint of this study is the mean change in best corrected visual acuity (BCVA) of Ixo-vec compared to an active comparator measured as an average at Weeks 52 and 56.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

• Neovascular Age-Related Macular Degeneration (nAMD)
• Wet AMD

Eligibility basics and study details

Study type

Interventional

Phase

Phase 3

Ages

50 years and older

Sex

All

Healthy volunteers

Not accepted

Sponsor

Adverum Biotechnologies, Inc.

Last updated on ClinicalTrials.gov

September 24, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites