Drug intelligence / Profile preview

AVB-307

Development stage
Preclinical
Lead developer
AviadoBio
Modality
AAV Vectors → Viral Vectors → Gene Addition/Replacement → Gene Therapies
Administration
Ophthalmic
01

Overview

AVB-307 is an investigational adeno-associated virus (AAV)-based optogenetic gene therapy being developed by AviadoBio for the treatment of inherited retinal diseases (IRDs). The therapy utilizes optogenetics to restore vision by delivering a gene encoding a light-sensitive protein (opsin) to specific retinal cells, such as bipolar or ganglion cells, effectively turning them into functional photoreceptors. This approach is designed to be mutation-agnostic, potentially benefiting patients with various forms of advanced retinal degeneration where photoreceptor cells have been lost but the downstream neural architecture remains intact. AVB-307 is intended to be delivered via intravitreal injection and aims to provide a durable, one-time treatment to restore light sensitivity and visual perception.

02

Targets

ChR2 (Channelrhodopsin-2)

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