Protein delivery opportunity
Many potentially useful therapeutic proteins cannot efficiently cross retinal cell membranes. Nuc1 is designed to address that bottleneck directly.
Core technology
Visiogene’s platform strategy combines engineered AAV delivery with a cell‑penetrating chaperone that expands the range of molecules that can be delivered to retinal cells.
AAV‑IKV
AAV‑IKV incorporates a short IKV sequence into an AAV9 capsid context, creating a vector designed for transgene delivery to outer retinal targets from an intravitreal route in preclinical studies.
Nuc1
Nuc1 is designed to engage retinal cell uptake and assist intracellular delivery of diverse cargo without requiring chemical conjugation.
Many potentially useful therapeutic proteins cannot efficiently cross retinal cell membranes. Nuc1 is designed to address that bottleneck directly.
Nuc1 has been used with AAV‑IKV to enhance ocular transduction in preclinical studies, providing a modular delivery layer.
The platform creates room for recombinant protein therapies, gene editing protein cargo, antibody delivery, and vector delivery strategies.
How the platforms fit together
AAV‑IKV is the durable transgene expression platform. Nuc1 is the delivery chaperone. Together, they support both owned product candidates and partnering applications.
Programs can target photoreceptors, RPE, and choroidal neovascularization biology through intravitreal delivery.
AAV‑IKV supports intracameral delivery hypotheses for glaucoma and infantile aphakic glaucoma biology.
Nuc1 may enable intracellular protein delivery strategies that are not practical with conventional intraocular biologics.
Science
Visiogene’s platform science supports a focused pipeline across retinal and anterior segment disease.