Retinal penetrating AAV for blinding disease

Delivering genetic medicines to ocular tissues that are difficult to reach.

Visiogene is a preclinical-stage biotechnology startup developing AAV‑IKV, a retinal‑penetrating AAV platform, and Nuc1, a protein and large‑molecule delivery chaperone, for diseases that cause blindness.

Vitreous to outer retinaAAV‑IKV retinal penetration
Decorin biologyFibrosis, CNV, and trabecular meshwork remodeling
Complement modulationUndisclosed dry AMD program
AAV-IKV vector pathway from the vitreous through retinal layers toward photoreceptors and retinal pigment epithelium

The eye provides local routes for administration, but retinal barriers still determine whether a therapeutic payload reaches photoreceptors, RPE, or outflow tissues.

Research package

Scientific focus

A delivery platform organized around defined ocular compartments.

The programs apply engineered delivery to compartments where disease biology is well characterized: the outer retina in macular degeneration and retinal degeneration, and the trabecular meshwork in glaucoma.

01

Retinal penetrating AAV

AAV‑IKV is designed for transgene delivery from the vitreous through retinal layers to outer retinal targets, including photoreceptors and RPE.

02

Wet AMD and fibrosis

AAV‑IKV‑Decorin studies address laser‑induced CNV and the fibrotic response, rather than treating angiogenesis as the only disease process.

03

Dry AMD complement

An undisclosed dry AMD program is focused on local complement modulation, building on Visiogene’s experience in complement biology for geographic atrophy.

04

Glaucoma outflow biology

AAV‑IKV‑Decorin is being studied for TGFβ2‑driven fibrosis at the trabecular meshwork, a mechanism linked to aqueous humor outflow resistance.

Platform emphasis

AAV‑IKV was developed to penetrate the retina from an intravitreal route.

The vector platform addresses a central constraint in ocular gene therapy: outer retinal cells are biologically important targets, but conventional vectors delivered into the vitreous generally have limited access to photoreceptors and RPE.

Read about AAV‑IKV
Intravitreal routeVector enters the vitreous
Retinal penetrationMovement across retinal barriers
Outer retinal expressionPhotoreceptors and RPE

AAV‑IKV also provides a delivery framework for anterior segment studies, including intracameral delivery to tissues involved in glaucoma pathophysiology.

Retinal disease program

Wet AMD studies directed at neovascularization and fibrosis.

The wet AMD program uses AAV‑IKV to deliver decorin, a matrix-associated proteoglycan with relevance to angiogenic, fibrotic, inflammatory, and autophagy pathways. The public preclinical work emphasizes both CNV and subretinal fibrosis.

Wet AMD program
CNV+vascular leakage biology
Fibrosis+TGFβ-related remodeling
AAV‑IKV‑Decorinpreclinical decorin expression
TGFβ2EMT and fibrosis
Trabecular meshworkoutflow resistance
Decorinanti‑fibrotic counter‑biology

Glaucoma program

Local gene delivery to fibrotic outflow tissue.

In glaucoma models, AAV‑IKV is used as the delivery layer and decorin as the therapeutic transgene. Endpoints include trabecular meshwork fibrosis, intraocular pressure, retinal ganglion cell integrity, and ocular tolerability observations.

Glaucoma science

Pipeline

Programs selected for delivery, payload biology, and ocular compartment fit.

Wet AMD

AAV‑IKV‑Decorin

Decorin delivery studied for effects on neovascularization, fibrosis, inflammation, and autophagy.

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Dry AMD

Undisclosed complement program

Novel local complement targeting for dry AMD, with target and construct details undisclosed.

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Glaucoma

AAV‑IKV‑Decorin

Anterior segment gene delivery focused on TGFβ2 / decorin biology and trabecular meshwork fibrosis.

View program →

Team

Ocular gene therapy, retinal disease models, and clinical perspective.

Visiogene’s team combines ocular genetics, AAV vector development, retinal degeneration model expertise, and clinical research perspective.

Team
Rajendra Kumar‑Singh, PhDFounder and CEO
Manish Mishra, PhDSenior Scientist
Tiffany Kolniak, MD, PhDClinical and Research Advisor