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Clinical Trial Report

Gene Therapy Trial Report

Summary

Safety and Tolerability Subretinal OPGx-001 for LCA5-Associated Inherited Retinal Degeneration (LCA5-IRD)


NCTID NCT05616793 (View at clinicaltrials.gov)
Description
Indication Leber Congenital Amaurosis - Type 5
Compound Name OPGx-LCA5 (AAV8.hLCA5)
Sponsor Opus Genetics, Inc
Funder Type Industry
Status
Recruiting
Enrollment Count 15

Therapy Information


Target Gene/Variant LCA5
Therapy Type Gene transfer
Therapy Route In-vivo
Mechanism of Action Functional gene replacement
Route of Administration Subretinal
Drug Product Type Viral vector
Target Tissue/Cell
Delivery System Viral transduction
Vector Type AAV8
Editor Type
Dose 1 Undisclosed low dose
Dose 2 Undisclosed medium dose
Dose 3 Undisclosed high dose
Dose 4
Dose 5

Study Record Dates


Current Stage Phase1, Phase2
Submit Date 2022-11-07
Completion Date 2028-01-30
Last Update 2024-07-01

Participation Criteria


Eligible Age >=13 Years
Standard Ages Child, Adult, Older adult
Eligible Sex ALL

Locations


No.of Trial Sites 1
Locations United States

Regulatory Information


Has US IND True
Recent Updates Received Rare Pediatric Disease Designation from FDA

Resources/Links