RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular Degeneration (nAMD)
- Conditions
- Wet Macular DegenerationWet Age-related Macular DegenerationNeovascular Age-related Macular Degeneration
- Interventions
- Genetic: RGX-314
- Registration Number
- NCT04832724
- Lead Sponsor
- AbbVie
- Brief Summary
RGX-314 is being developed as a novel one-time gene therapy for the treatment of neovascular (wet) age-related macular degeneration (nAMD) also referred to as Wet AMD. Wet AMD is characterized by loss of vision due to new, leaky blood vessel formation in the retina. The purpose of this phase 2, open label study is to evaluate whether different doses of RGX-314 from two different formulations (clinical versus eventual commercial formulation) perform the same in humans when delivered by subretinal administration
- Detailed Description
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-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 repeated intraocular injections to maintain efficacy. Due to the burden of treatment, patients often experience a decline in vision with reduced frequency of treatment over time. RGX-314 is being developed as a potential one-time treatment for wet AMD. RGX-314 uses an AAV8 vector that contains a gene that encodes for a monoclonal antibody fragment which binds to and neutralizes VEGF activity. This phase 2, open label study will explore the pharmacodynamics of two doses in two formulations of RGX-314 gene therapy via subretinal delivery in patients with neovascular Age-related Macular Degeneration. Approximately 60 patients (15 per cohort) who meet the inclusion/exclusion criteria will be enrolled in 4 sequential dose cohorts. A dose cohort will be comprised of 1 of 2 doses of RGX-314 in 1 of 2 formulations in order to explore the pharmacodynamics of RGX-314 based on aqueous humor transgene product (TP) concentrations. If the participants meet the study criteria and choose to participate in the study, their participation in the study will last about 12 months.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
- Males or females, aged ≥ 50 years and ≤ 89 years.
- An Early Treatment Diabetic Retinopathy Study (ETDRS) BCVA-letter score between ≤ 78 and ≥ 40 in the study eye at Screening.
- Diagnosis of choroidal neovascularization (CNV) secondary to age-related macular degeneration in the study eye previously treated with anti-VEGF.
- Participants must have demonstrated a meaningful response to anti-VEGF therapy at study entry.
- Willing and able to provide written, signed informed consent for this study.
- Must be pseudophakic (at least 12 weeks postcataract surgery) in the study eye.
- CNV or macular edema in the study eye secondary to any causes other than AMD.
- Subfoveal fibrosis or atrophy in study eye.
- Any condition in the investigator's opinion that could limit visual acuity improvement in the study eye.
- Active or history of retinal detachment or retinal tear in the study eye.
- Advanced glaucoma in the study eye.
- Prior treatment with gene therapy.
- Myocardial infarction, cerebrovascular accident, or transient ischemic attack within the past 6 months.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description Commercial Formulation Dose 1 RGX-314 Dose 1 of RGX-314 Commercial Formulation Dose 2 RGX-314 Dose 2 of RGX-314 Clinical Formulation Dose 2 RGX-314 Dose 2 of RGX-314 Clinical Formulation Dose 1 RGX-314 Dose 1 of RGX-314
- Primary Outcome Measures
Name Time Method RGX-314 target protein concentration in aqueous humor At Week 24
- Secondary Outcome Measures
Name Time Method Incidence and severity of ocular Adverse Events (AEs) and overall AEs Through Week 48 Evaluate the safety and tolerability of RGX-314
Changes in Central Retinal Thickness (CRT) At Week 24 and 48 CRT is measured by spectral domain optical coherence tomography (SD-OCT)
Changes in Best Corrected Visual Acuity (BCVA) At Week 24 and 48 BCVA measured by Early Treatment Diabetic Retinopathy Study (ETDRS)
Mean Supplemental anti-VEGF injection annualized rate through week 24 and week 48 Through Week 24 and week 48 To assess the need for supplemental anti-VEGF therapy over 48 weeks
Trial Locations
- Locations (13)
Wilmer Eye Institute
🇺🇸Baltimore, Maryland, United States
Retina Consultants of Texas
🇺🇸The Woodlands, Texas, United States
California Retina Consultants
🇺🇸Santa Barbara, California, United States
Sierra Eye Associates
🇺🇸Reno, Nevada, United States
Wills Eye Hospital
🇺🇸Philadelphia, Pennsylvania, United States
Retina Consultants of San Diego
🇺🇸San Diego, California, United States
Eye Associates of New Mexico
🇺🇸Albuquerque, New Mexico, United States
Texas Retina Associates
🇺🇸Dallas, Texas, United States
Retina Vitreous Associates of Florida
🇺🇸Saint Petersburg, Florida, United States
Retinal Consultants of Arizona
🇺🇸Phoenix, Arizona, United States
Ophthalmic Consultants of Boston
🇺🇸Boston, Massachusetts, United States
Barnet Dulaney Perkins Eye Center
🇺🇸Sun City, Arizona, United States
Charles Retina Institute
🇺🇸Germantown, Tennessee, United States