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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT06856577

Public ClinicalTrials.gov record NCT06856577. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 9:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Double-Masked, Active-Comparator-Controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Ixoberogene Soroparvovec (Ixo-vec) in Participants With Neovascular Age-Related Macular Degeneration (ARTEMIS)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 an 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 at an average of Weeks 52 and 56. Safety, tolerability, and efficacy will be evaluated throughout the study.

Study identification

NCT ID
NCT06856577
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Adverum Biotechnologies, Inc.
Industry
Enrollment
311 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 28, 2025 (Actual)
Primary completion
Dec 22, 2026 (Estimated)
Completion
Nov 23, 2030 (Estimated)
Last update posted
May 22, 2026

2025 – 2030

United States locations

U.S. sites
75
U.S. states
23
U.S. cities
70
Facility City State ZIP Site status
Adverum Clinical Site 223 Gilbert Arizona 85297 —
Adverum Clinical Site 178 Phoenix Arizona 85021 —
Adverum Clinical Site 126 Phoenix Arizona 85053 —
Adverum Clinical Site 229 Scottsdale Arizona 85255 —
Adverum Clinical Site 159 Tucson Arizona 85704 —
Adverum Clinical Site 198 Springdale Arkansas 72764 —
Adverum Clinical Site 109 Bakersfield California 93309 —
Adverum Clinical Site 100 Beverly Hills California 90211 —
Adverum Clinical Site 201 Campbell California 95008 —
Adverum Clinical Site 172 Encino California 91436 —
Adverum Clinical Site 169 Fullerton California 92835 —
Adverum Clinical Site 224 Huntington Beach California 92647 —
Adverum Clinical Site 215 Redlands California 92374 —
Adverum Clinical Site 164 Riverside California 92505 —
Adverum Clinical Site 140 Sacramento California 95825 —
Adverum Clinical Site 212 Sacramento California 95841 —
Adverum Clinical Site 175 Santa Barbara California 93103 —
Adverum Clinical Site 202 Torrance California 90503 —
Adverum Clinical Site 189 Walnut Creek California 94598 —
Adverum Clinical Site 200 Denver Colorado 80222 —
Adverum Clinical Site 116 Lakewood Colorado 80228 —
Adverum Clinical Site 165 Waterford Connecticut 06385 —
Adverum Clinical Site 184 Deerfield Beach Florida 33064 —
Adverum Clinical Site 176 Fort Lauderdale Florida 33308 —
Adverum Clinical Site 221 Fort Myers Florida 33912 —
Adverum Clinical Site 168 Jacksonville Florida 32216 —
Adverum Clinical Site 214 Lakeland Florida 33805 —
Adverum Clinical Site 213 Orlando Florida 32806 —
Adverum Clinical Site 230 Pensacola Florida 32503 —
Adverum Clinical Site 124 Pompano Beach Florida 33064 —
Adverum Clinical Site 183 South Miami Florida 33143 —
Adverum Clinical Site 120 St. Petersburg Florida 33711 —
Adverum Clinical Site 193 Tampa Florida 33617 —
Adverum Clinical Site 182 Augusta Georgia 30909 —
Adverum Clinical Site 179 Oak Forest Illinois 60452 —
Adverum Clinical Site 207 Oak Park Illinois 60304 —
Adverum Clinical Site 195 Carmel Indiana 46032 —
Adverum Clinical Site 205 Carmel Indiana 46032 —
Adverum Clinical Site 197 Hagerstown Maryland 21740 —
Adverum Clinical Site 204 Hagerstown Maryland 21740 —
Adverum Clinical Site 167 Detroit Michigan 48201 —
Adverum Clinical Site 216 Madison Mississippi 39110 —
Adverum Clinical Site 163 Southaven Mississippi 38671 —
Adverum Clinical Site 190 St Louis Missouri 63128 —
Adverum Clinical Site 171 Teaneck New Jersey 07666 —
Adverum Clinical Site 225 Liverpool New York 13088 —
Adverum Clinical Site 196 Asheville North Carolina 28803 —
Adverum Clinical Site 234 Cary North Carolina 27511 —
Adverum Clinical Site 186 Durham North Carolina 27705 —
Adverum Clinical Site 211 Greensboro North Carolina 27401 —
Adverum Clinical Site 220 Hickory North Carolina 28602 —
Adverum Clinical Site 209 Wake Forest North Carolina 27587 —
Adverum Clinical Site 219 Winston-Salem North Carolina 27103 —
Adverum Clinical Site 181 Erie Pennsylvania 16507 —
Adverum Clinical Site 110 Philadelphia Pennsylvania 19107 —
Adverum Clinical Site 208 Charleston South Carolina 29414 —
Adverum Clinical Site 222 Ladson South Carolina 29456 —
Adverum Clinical Site 122 West Columbia South Carolina 29169 —
Adverum Clinical Site 144 Rapid City South Dakota 57701 —
Adverum Clinical Site 123 Abilene Texas 79606 —
Adverum Clinical Site 127 Austin Texas 78705 —
Adverum Clinical Site 108 Bellaire Texas 77401 —
Adverum Clinical Site 227 Burleson Texas 76028 —
Adverum Clinical Site 194 Dallas Texas 75231 —
Adverum Clinical Site 188 Houston Texas 77030 —
Adverum Clinical Site 218 Katy Texas 77494 —
Adverum Clinical Site 162 McAllen Texas 78503 —
Adverum Clinical Site 185 San Antonio Texas 78240 —
Adverum Clinical Site 232 San Marcos Texas 78666 —
Adverum Clinical Site 228 Schertz Texas 78154 —
Adverum Clinical Site 107 The Woodlands Texas 77384 —
Adverum Clinical Site 231 The Woodlands Texas 77384 —
Adverum Clinical Site 199 Lynchburg Virginia 24502 —
Adverum Clinical Site 131 Spokane Washington 99204 —
Adverum Clinical Site 187 Wausau Wisconsin 54403 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06856577, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 22, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06856577 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →