Age-Related Macular Degeneration (ARMD) Clinical Trials

Find Age-Related Macular Degeneration (ARMD) Clinical Trials Near You

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An Investigator-initiated, Open-label, Dose-escalation Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of HG005 in Pediatric Patients With Stargardt Disease (STGD1) Caused by Biallelic ABCA4 Mutations

Status: Recruiting
Location: See location...
Intervention Type: Genetic
Study Type: Interventional
Study Phase: Early Phase 1
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
Participation Requirements
Sex: All
Minimum Age: 6
Maximum Age: 17
Healthy Volunteers: f
View:

• Patient ≥ 6 and ≤17 years at the time of signing informed consent, with clinical diagnosis of Stargardt disease;

• At least one ABCA4 allele on each chromosome;

• Both eyes must have well-defined macular atrophic lesions consistent with the diagnosis 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 required eye examination.

Locations
Other Locations
China
Eye & ENT Hospital of Fudan University
RECRUITING
Shanghai
Contact Information
Primary
Study Director
HG00501@huidagene.com
+86 021-25076143
Time Frame
Start Date: 2025-08-20
Estimated Completion Date: 2028-02-28
Participants
Target number of participants: 6
Treatments
Experimental: HG005
The study will enroll up to 2 dose cohorts
Related Therapeutic Areas
Late-Onset Retinal Degeneration
Stargardt Macular Degeneration
Age-Related Macular Degeneration (ARMD)
Sponsors
Leads: HuidaGene Therapeutics Co., Ltd.

This content was sourced from clinicaltrials.gov

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