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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 Sep 2, 2026, 5:34 AM 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 27, 2025
Primary completion
Dec 21, 2026
Completion
Nov 22, 2030
Last update posted
May 21, 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 21, 2026 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06856577 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →