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Study identifier: NCT07007065 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Assess the Injection Burden, Adverse Events, Change in Disease Activity, and Long-Term Preservation of Visual Acuity of Surabgene Lomparvovec in Adult Participants With Neovascular Age-Related Macular Degeneration (nAMD)

Condition: Neovascular Age-related Macular Degeneration  ·  Sponsor: AbbVie

PhasePhase 3
Planned participants561
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

Neovascular age-related macular degeneration (nAMD), also known as "wet" AMD, is the abnormal growth of new blood vessels in the light-sensitive tissue at the back of the eye called the retina. The purpose of this study is to assess how safe and effective Surabgene Lomparvovec is in treating participants with Neovascular age-related macular degeneration (nAMD). Surabgene Lomparvovec (ABBV-RGX-314) is an investigational gene therapy being developed for the treatment of neovascular age-related macular degeneration (nAMD). Participants will be placed into 1 of 3 groups, called treatment arms. Each group receives different treatment. Adult participants aged 50 and older years with a diagnosis of previously treated nAMD will be enrolled. Around 561 participants will be enrolled in the study at approximately 150 sites worldwide. Participants in groups 1 and 2 will receive a single subretinal dose of ABBV-RGX-314. Participants in group 3 will receive Ranibizumab as needed throughout the study. Ranibizumab will be given as an intravitreal injection (injection into the jelly-like tissue that fills the eyeball injection), and ABBV-RGX-314 will be given as a subretinal (between the retina and the back of the eye) injection. The Assessment Period begins after randomization (1:1:1) to one of the ABBV-RGX-314 treatment groups or control at Week -2 and lasts up to 5 years. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants…

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (129)

Barnet Dulaney Perkins Eye Centers /ID# 279265Mesa, Arizona, United StatesRecruiting
American Vision Partners /ID# 264615Sun City, Arizona, United StatesRecruiting
Retinal Diagnostic Center /ID# 263054Campbell, California, United StatesRecruiting
The Retina Partners /ID# 263265Encino, California, United StatesRecruiting
Retina Associates of Southern California /ID# 263056Huntington Beach, California, United StatesRecruiting
Northern California Retina Vitreous Associates - Mountain View /ID# 263990Mountain View, California, United StatesRecruiting
Retina Consultants of San Diego /ID# 264026Poway, California, United StatesRecruiting
Retina Consultants Of Southern California - Redlands /ID# 276496Redlands, California, United StatesRecruiting
Kaiser Permanente - Riverside Medical Center /ID# 263253Riverside, California, United StatesRecruiting
Retinal Consultants - Sacramento - Greenback Lane /ID# 263983Sacramento, California, United StatesRecruiting
UCSF, Wayne and Gladys Valley Center for Vision /ID# 263058San Francisco, California, United StatesRecruiting
Orange County Retina Medical Group /ID# 266612Santa Ana, California, United StatesRecruiting

+ 117 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT07007065