Contact SCGE
Your email
Message
Send
SCGE Consortium Home
|
About SCGE TCDC
|
Contact Us
|
License
Home
Gene Therapy Trial Browser
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
The goal of this clinical trial is to evaluate the safety and preliminary efficacy of subretinal gene therapy with OPGx-001 in patients with inherited retinal degeneration due to biallelic mutations in the LCA5 gene.
(Show More)
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
News and Press Releases
https://opusgtx.com/companynews/opus-genetics-receives-rare-pediatric-disease-designation-from-the-u-s-fda-for-ocular-gene-therapy-opgx-lca5-to-treat-rare-inherited-retinal-disease-lca5/
Preclinical Publications
PMID: 32428231