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  • Safety and Efficacy Trial of AAV Gene Therapy in Patients With CNGA3 Achromatopsia (A Clarity Clinical Trial)

Safety and Efficacy Trial of AAV Gene Therapy in Patients With CNGA3 Achromatopsia (A Clarity Clinical Trial)

Principal Investigator

Byron Lam

Enrollment Status

Not Accepting

Clinical Trial ID

Institutional Protocol # 20160984
National Clinical Trials Identifier NCT02935517

Clinical Trial Summary

This will be a non-randomized, open-label, Phase 1/2 study of the safety and efficacy of
AGTC-402, administered to one eye by subretinal injection in individuals with achromatopsia
caused by mutations in the CNGA3 gene. The primary study endpoint will be safety and the
secondary study endpoint will be efficacy.


Phase

Phase 1/Phase 2


Funding Agency/Sponsor

Industry


Disease

Other


Enrollment Eligibility

Inclusion Criteria:
1. Male or female subjects with documented mutations in both alleles of the CNGA3 gene;
2. Retinal disease consistent with a clinical diagnosis of achromatopsia;
3. At least 18 years of age for Groups 1, 2, 3, 4, and 5. At least 6 years of age for
Group 3a, and and 4-8 years of age for Groups 4a and 6;
4. Able to perform tests of visual and retinal function;
5. Visual acuity in the study eye not better than 55 ETDRS letters (Snellen equivalent
20/80) based on the average of two examinations at the baseline visit;
6. Acceptable laboratory parameters;
7. For females of childbearing potential: A negative pregnancy test within 2 days before
administration of study agent.
Exclusion Criteria include:
1. Best-corrected visual acuity difference between the two eyes of > 15 ETDRS letters (3
lines);
2. Evidence of degenerative myopia in the study eye;
3. Pre-existing eye conditions that would contribute to vision loss in either eye or
increase the risk of subretinal injection in the study eye.


Contact Information

Study Contact Potyra Rosa
Phone Number +1 (305) 4824584
Email prosa@miami.edu
Get detailed information on ClinicalTrials.Gov

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