Drug intelligence / Profile preview

rAAV2.7m8-VEGF decoy receptor

Development stage
Preclinical
Lead developer
Tehran University of Medical Sciences
Modality
Gene Therapies
Administration
Intravitreal
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Overview

rAAV2.7m8-VEGF decoy receptor is an experimental gene therapy candidate designed for the treatment of neovascular age-related macular degeneration (nAMD). It utilizes a recombinant adeno-associated virus (AAV) vector with the 2.7m8 capsid, which is engineered for enhanced retinal penetration and transduction following intravitreal delivery. The vector carries a transgene encoding a high-affinity vascular endothelial growth factor (VEGF) decoy receptor, driven by a CMV promoter/enhancer cassette. This approach aims to provide sustained intraocular production of a VEGF inhibitor, potentially reducing the treatment burden associated with frequent anti-VEGF injections. Preclinical studies in rat models have demonstrated that a single intravitreal administration significantly suppresses laser-induced choroidal neovascularization (CNV) with efficacy comparable to aflibercept and no evidence of ocular structural damage.

02

Targets

VEGFA (Vascular endothelial growth factor A)VEGFB (Vascular endothelial growth factor B)FCGRT (Neonatal crystallizable fragment receptor)PGF (Placental Growth Factor)

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