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Clinical Trials in Germany / NCT05407636
Active, not recruiting Phase 3

Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD

NCT05407636 · tracked via the Priya Life Science Germany tracker
Sponsor
Phase
Phase 3
Started
2022-01-13
Last updated
2026-08-03

Condition(s) studied

AMDnAMDWet Age-related Macular DegenerationwAMDWetAMDCNV

Investigational drug(s) / intervention(s)

ABBV-RGX-314 Dose 1ABBV-RGX-314 Dose 2Aflibercept (EYLEA®) →

ABBV-RGX-314 Dose 1: AAV8 vector containing a transgene for anti-VEGF Fab (Dose 1)

ABBV-RGX-314 Dose 2: AAV8 vector containing a transgene for anti-VEGF Fab (Dose 2)

Aflibercept (EYLEA®): 2.0 mg (0.05 mLsolution) administered by intravitreal injection approximately every 8 weeks after 3 monthly injections

Study summary

ABBV-RGX-314 (also known as RGX-314 and surabgene lomparvovec (sura-vec)) is being developed as a novel one-time gene therapy for the treatment of neovascular (wet) age-related macular degeneration (wet AMD). Wet AMD is characterized by loss of vision due to new, leaky blood vessel formation in the retina. Wet AMD is a significant cause of vision loss in the United States, Europe and Japan, with up to 2 million people living with wet AMD in these geographies alone. Current anti-vascular endothelial growth factor (VEGF) therapies have significantly changed the landscape for treatment of wet AMD, becoming the standard of care due to their ability to prevent progression of vision loss in the majority of patients. These therapies, however, require life-long intraocular injections, typically repeated every four to 12 weeks in frequency, to maintain efficacy. Due to the burden of treatment, patients often experience a decline in vision with reduced frequency of treatment over time. ABBV-RGX-314 is being developed as a potential one-time treatment for wet AMD.

Eligibility

Sex
ALL
Min age
50 Years
Max age
89 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age ≥ 50 years and ≤ 89 years 2. An ETDRS BCVA letter score between ≤ 78 and ≥ 40 in the study eye 3. Diagnosis of subfoveal choroidal neovascularization (CNV) secondary to AMD in the study eye previously treated with anti-VEGF 4. Must be pseudophakic (at least 12 weeks postcataract surgery) in the study eye 5. Willing and able to provide written, signed informed consent for this study 6. Participants must have demonstrated a meaningful response to anti-VEGF therapy at study entry Inclusion Criteria (Bilateral Treatment Substudy)\*: 1. An ETDRS BCVA letter score between ≤ 83 and ≥ 40 in both eyes 2. Diagnosis of subfoveal choroidal neovascularization (CNV) secondary to AMD in both eyes 3. Must be pseudophakic (at least 12 weeks postcataract surgery) in both eyes 4. Willing and able to provide written, signed informed consent for this study 5. Newcomers must have active disease in the study eye; crossover participants must have active disease in the eye not treated in the main study Exclusion Criteria: 1. CNV or macular edema in the study eye secondary to any causes other than AMD 2. Subfoveal fibrosis or atrophy in the study eye 3. Any condition in the investigator's opinion that could limit VA improvement in the study eye 4. Advanced glaucoma or history of secondary glaucoma in the study eye 5. Myocardial infarction, cerebrovascular accident, or transient ischemic attack within the past 6 months 6. History of intraocular surgery in the study eye within 12 weeks prior to randomization 7. History of intravitreal therapy in the study eye, such as intravitreal steroid injection or investigational medicinal product, other than an intravitreal therapy for AMD, in the 6 months prior to Week -6 8. Prior treatment with gene therapy Exclusion Criteria (Bilateral Treatment Substudy)\*: 1. CNV or macular edema in either eye secondary to any causes other than AMD 2. Subfoveal fibrosis or atrophy in either eye 3. Any condition in the investigator's opinion that could limit VA improvement in either eye 4. Advanced glaucoma or history of secondary glaucoma in either eye 5. Myocardial infarction, cerebrovascular accident, or transient ischemic attack within the past 6 months 6. History of intraocular surgery in either eye within 12 weeks prior to randomization 7. History of intravitreal therapy in the study eye, such as intravitreal steroid injection or investigational medicinal product, other than an intravitreal therapy for AMD, in the 6 months prior to Week -6. 8. Prior treatment with gene therapy (\*) For previously treated crossover participants, criteria apply to the eye not treated in the main study only. Note: Other inclusion/exclusion criteria apply

Primary outcome measure(s)

Trial sites (181)

FacilityCityRegionStatus
Barnet Dulaney Eye Center-Phoenix /ID# 256340 Phoenix Arizona
Retinal Research Institute /ID# 256238 Phoenix Arizona
Retina Macula Institute of Arizona /ID# 271026 Scottsdale Arizona
California Retina Consultants - Bakersfield /ID# 256240 Bakersfield California
Retina Vitreous Assoc Med Grp /ID# 256246 Beverly Hills California
Retinal Diagnostic Center /ID# 256262 Campbell California
The Retina Partners - Encino /ID# 259660 Encino California
Retina Consultants of Orange County /ID# 256267 Fullerton California
Jacobs Retina Center at UCSD/ID# 256320 La Jolla California
California Retina Consultants - Oxnard - North Ventura Road /ID# 262883 Oxnard California
Byers Eye Institute Stanford /ID# 262853 Palo Alto California
Retina Consultants of San Diego /ID# 256258 Poway California
Kaiser Permanente - Riverside Medical Center /ID# 262413 Riverside California
UC Davis Health Eye Center Sacramento California
Retinal Consultants Medical Group, Inc. - Greenback /ID# 256353 Sacramento California
Orange County Retina Medical Group /ID# 256286 Santa Ana California
Macula Retina Vitreous Center - Torrance /ID# 270247 Torrance California
Bay Area Retina Associates - Walnut Creek - Lennon Lane /ID# 268513 Walnut Creek California
Retina Consultants of Southern Colorado /ID# 256285 Colorado Springs Colorado
Southwest Retina Research Center /ID# 256261 Durango Colorado
Colorado Retina Associates /ID# 256378 Lakewood Colorado
Advanced Vision Research Institute /ID# 256380 Longmont Colorado
Retina Consultants, P.C. /ID# 273610 Manchester Connecticut
Rand Eye Institute /ID# 256337 Deerfield Beach Florida
National Ophthalmic Research Institute /ID# 256344 Fort Myers Florida
Vitreoretinal Associates, P.A. /ID# 256266 Gainesville Florida
Florida Retina Consultants /ID# 256321 Lakeland Florida
Florida Retina Institute - Orlando /ID# 256373 Orlando Florida
Retina Specialty Institute /ID# 256268 Pensacola Florida
Fort Lauderdale Eye Institute /ID# 266011 Plantation Florida
Retina Vitreous Associates of Florida - St. Petersburg /ID# 256279 St. Petersburg Florida
Center for Retina and Macular Disease /ID# 256335 Winter Haven Florida
Georgia Retina - Marietta /ID# 256264 Marietta Georgia
Retina Consultants of Hawaii /ID# 256278 ‘Aiea Hawaii
Northwestern Memorial Hospital - Department of Ophthalmology /ID# 256379 Chicago Illinois
University Retina and Macula Associates /ID# 256288 Lemont Illinois
University Retina and Macula Associates /ID# 256287 Oak Forest Illinois
Illinois Retina Associates - Oak Park /ID# 256375 Oak Park Illinois
Springfield Clinic - First /ID# 256371 Springfield Illinois
Retina Partners Midwest, PC /ID# 256277 Indianapolis Indiana

+ 141 more sites — see the full list on the official registry below.

More AbbVie trials in Germany

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05407636 on ClinicalTrials.gov ↗ ← All trials in Germany