Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space for Participants With and Without Diabetic Retinopathy
← catalyst calendarNCT05296447 · readout ≤ 1,776 d
Sponsored by AbbVie (industry) · ABBV — their whole pipeline →. With REGENXBIO Inc..
Phase
Phase 2
Status
Enrolling by invitation
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
100estimated
Sites
20
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2022-04-04 | actual | When the study began enrolling |
| Primary completion | Jun 2031 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Jun 2031 | estimated | The whole study's end, after follow-up |
| First posted | 2022-03-25 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-05 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Diabetic Retinopathy, DR
Interventions
- Drug: Standard of Care
- Drug: Aflibercept — also filed as EYLEA
Primary outcome
what the primary-completion date above is the date OFIncidence of ocular adverse events (AEs) and any serious adverse events (SAEs)
measured 5 years inclusive of the parent study
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