A Long-term Follow-Up Study to Evaluate the Safety | Clinical Research Studies Listing

Recruiting

99 years or below

All

1 Location

Brief description of study

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 in which they received a single subretinal administration of RGX-314 (IRB #827859). Participants will be followed for up to 5 years post-RGX-314 administration (inclusive of the parent study).

Eligibility of study

You may be eligible for this study if you meet the following criteria:

Conditions: Medical Research
Age: 99 years or below
Gender: All

Updated on 12 Apr 2023. Study ID: 833581

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A Long-term Follow-Up Study to Evaluate the Safety and Efficacy of RGX-314

Brief description of study

Eligibility of study

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