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Clinical Trial Summary

This is a prospective, observational study designed to evaluate the long-term safety and efficacy of RGX-314. Eligible participants are those who were previously enrolled in a clinical study of nAMD in which they received suprachoroidal space (SCS) administration of RGX-314. Enrollment of each participant in the current study should occur after the participant has completed either the end of study or early discontinuation visit in the previous (parent) clinical study. Participants will be followed for up to 5 years after RGX-314 administration (inclusive of the parent study). As such, the total study duration for each participant may vary depending on when they enroll in the current study following RGX-314 administration in the parent study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05210803
Study type Observational
Source Regenxbio Inc.
Contact
Status Enrolling by invitation
Phase
Start date December 20, 2021
Completion date May 7, 2027

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