ROCKVILLE, Md., Oct. 18,
2024 /PRNewswire/ -- REGENXBIO Inc. (Nasdaq: RGNX)
today announced that it will present new interim data evaluating
subretinal delivery of ABBV-RGX-314 in patients with bilateral wet
age-related macular degeneration (wet AMD) at the American Academy
of Ophthalmology 2024 annual meeting. ABBV-RGX-314 is an
investigational one-time AAV Therapeutic being developed in
collaboration with AbbVie for the treatment of wet AMD, diabetic
retinopathy and other additional chronic retinal conditions.
New data will be presented as follows:
Title: Subretinal Delivery of Investigational
ABBV-RGX-314 as a Gene Therapy for nAMD: First Time Results of a
Fellow Eye Bilateral Dosing Study (abstract 30080148)
Presenter: Arshad Khanani
M.D., M.A., FASRS, Director of Clinical Research at Sierra
Eye Associates
Date/Time: Saturday, October 19,
2024, at 11:59 a.m. ET
Encore presentations will be presented as follows:
Title: A Phase 2 Dose-Escalation Study Evaluating
Suprachoroidal Delivery of Investigational ABBV-RGX-314 Gene
Therapy for DR (abstract 30078795)
Presenter: Arshad Khanani
M.D., M.A., FASRS, Director of Clinical Research at Sierra
Eye Associates
Date/Time: Monday, October 21,
2024, at 10:45 a.m. ET
Title: Long-Term Follow-Up Study Results from the
Investigational Phase I/IIa ABBV-RGX-314 Subretinal Delivery Gene
Therapy Program in nAMD (abstract 30079480)
Presenter: Philip P. Storey,
M.D., Austin Retina Associates
Date/Time: Monday, October 21,
2024, at 12:45 p.m. ET
About REGENXBIO Inc.
REGENXBIO is a leading
clinical-stage biotechnology company seeking to improve lives
through the curative potential of gene therapy. Since its founding
in 2009, REGENXBIO has pioneered the development of AAV
Therapeutics, an innovative class of gene therapy medicines.
REGENXBIO is advancing a pipeline of AAV Therapeutics for retinal
and rare diseases, including ABBV-RGX-314 for the treatment of wet
AMD and diabetic retinopathy, being developed in collaboration with
AbbVie, RGX-202 for the treatment of Duchenne and RGX-121 for the
treatment of MPS II. Thousands of patients have been treated with
REGENXBIO's AAV Therapeutic platform, including Novartis' ZOLGENSMA
for children with spinal muscular atrophy. Designed to be one-time
treatments, AAV Therapeutics have the potential to change the way
healthcare is delivered for millions of people. For more
information, please visit www.regenxbio.com.
Zolgensma® is a registered trademark of Novartis Gene
Therapies.
Contacts:
Dana
Cormack
Corporate Communications
DCORMACK@regenxbio.com
George E. MacDougall
Investor Relations
IR@regenxbio.com
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