An Clinical Study Evaluating the Safety, Tolerability, and efficAcy of HG005 in StaRgardT Disease

Phase

Condition

Macular Degeneration

Myopic Macular Degeneration

Geographic Atrophy

Treatment

HG005

Clinical Study ID

NCT07063251

HG00501

Ages 6-17
All Genders

Study Summary

Stargardt disease type 1 (STGD1) is a rare genetic eye condition that causes progressive vision loss, often beginning in childhood or adolescence. It is the most common form of inherited macular degeneration and can lead to legal blindness. STGD1 is caused by mutations in the ABCA4 gene, which normally helps clear waste from the photoreceptor cells in the retina. When ABCA4 gene doesn't function properly, toxic substances like A2E accumulate and damage the retinal pigment epithelium (RPE), leading to vision loss.

There are currently no approved treatments for STGD1. HG005 is an investigational gene therapy designed to deliver a healthy copy of the ABCA4 gene to the retina. Because the gene is too large to fit into a single AAV (adeno-associated virus) vector, HG005 used two AAV vectors that work together in retinal cells to produce the full-length, functional ABCA4 protein. The goal of HG005 is to restore normal waste removal, protect retinal cells from further damage, and slow or stop vision loss.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Patient ≥ 6 and ≤17 years at the time of signing informed consent, with clinicaldiagnosis of Stargardt disease;
At least one ABCA4 allele on each chromosome;
Both eyes must have well-defined macular atrophic lesions consistent with thediagnosis of Stargardt macular dystrophy.
Meet visual acuity criteria based on ETDRS letter chart
Subject must agree to contraception during the study.
Acceptable hematology, clinical chemistry, urine laboratory, and protocol requiredeye examination.

Exclusion

Exclusion Criteria:

Presence of active intraocular inflammation or uveitis history in either eye;
Presence of ocular or periocular infection history in either eye within 2 weeksprior to selection;
History or presence of corneal dystrophy in the study eye;
History of HIV or hepatitis A, B, or C infection;
Previous treatment with any gene therapy or cell therapy (e.g., stem celltransplantation);
Additional intraocular surgery in study eye 3 months prior to baseline visit;
Participation in an oral therapeutic STGD clinical trial within 3 months (or within 5 half-lives after last dose) prior to Screening
Any concomitant treatment that, in the opinion of the investigator, might interferewith the surgical procedure or healing process of the eye
Any other conditions that would not allow the potential subject to completefollow-up examinations during the study and would, in the opinion of theinvestigator, make the potential subject unsuitable for the study.

Study Design