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Elisigen Announces Presentation at 44th Annual Scientific Meeting of the American Society of Retina Specialists

July 13, 2026

SEOUL, South Korea, July 13, 2026 - Elisigen, a clinical-stage biotechnology company developing AAV gene therapies for ophthalmology and neurology, today announced a podium presentation at the 44th Annual Scientific Meeting of the American Society of Retina Specialists (ASRS) being held in Montreal, Canada, from July 15 - 18, 2026. The presentation will feature 44-week interim results from the medium-dose cohort (Cohort 2) of the Phase 1/2a clinical trial evaluating NG101, an investigational subretinal AAV gene therapy for wet age-related macular degeneration (wet AMD).

 

ASRS 2026 Presentation Details:

Title: One-Year First-in-Human Safety and Efficacy Data of Subretinal NG101 - A Novel Low-Dose AAV Gene Therapy for Wet AMD: A Phase 1/2a Clinical Trial

Date/Time: Thursday, July 16, 2026 (8:15 a.m. EDT)

Presenter: Peter J. Kertes, MD, FRCS(C), Professor and Chair Department of Ophthalmology and Vision Sciences, The University of Toronto

Session: AMD-Neovascular Panel. Beyond anti-VEGF: Emerging Durable Therapies in Neovascular AMD.

 

This presentation session showcases the latest clinical results of next-generation therapies that go beyond conventional anti-VEGF treatment, featuring a pipeline of high-dose protein therapeutic, bispecific antibody, sustained-release implant, and AAV gene therapies.

 

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Title

Speaker

1

Efficacy and safety of aflibercept 8 mg in previously treated patients with nAMD or DME: 24-week results from the phase 3b ELARA trial

Eric Schneider, MD

2

Results of a Randomized, Proof-of-Concept Clinical Trial Comparing OLN324 with Faricimab in Patients with Neovascular Age-Related Macular Degeneration

David Eichenbaum, MD, FASRS

3

Intravitreal Axitinib Hydrogel (OTX-TKI) in Neovascular Age-Related Macular Degeneration: Efficacy and Safety Results from the Phase 3 SOL-1 Trial

Dilsher Dhoot, MD

4

One-year, First-in-Human, Safety and Efficacy Data for Subretinal NG101 – a Novel Low-dose AAV Gene Therapy for Wet AMD: A Phase 1/2a Clinical Trial

Peter Kertes, MD, FRCS(C)

5

Ixoberogene soroparvovec (Ixo-vec) intravitreal gene therapy for neovascular age-related macular degeneration (nAMD): LUNA trial 2-year results

Shawn Kavoussi, MD

 

About NG101

NG101 is an investigational subretinal AAV gene therapy for wet AMD. It is designed to provide sustained anti-VEGF expression under Elisigen’s proprietary CAT311 promoter, with the goal of durable disease control from a single administration at a substantially lower vector dose. A Phase 1/2a open-label study is ongoing in the United States and Canada. The U.S. Food and Drug Administration has granted Fast Track designation for NG101 for the treatment of wet AMD.

 

About Elisigen

Elisigen is a clinical-stage biotechnology company developing AAV gene therapies for ophthalmology and neurology. Proprietary platforms include the CAT311 promoter for high-efficiency transgene expression and the Helper-In-One (dual-plasmid) system for high-yield AAV vector production. The company is headquartered in Seoul, Korea.

 

Contacts:

IR@elisigen.com