Drug intelligence / Profile preview

Nucleostim-VEGF

Development stage
Unknown
Lead developer
Histograft
Modality
Gene Therapies
Administration
Topical
01

Overview

Nucleostim-VEGF is a first-in-class gene-activated bone substitute developed by Histograft Co., Ltd. for the treatment of maxillofacial bone defects and alveolar ridge atrophy. The product consists of an octacalcium phosphate (OCP) scaffold combined with plasmid DNA encoding vascular endothelial growth factor (VEGF-A, specifically the VEGF165 isoform). Upon surgical implantation into a bone defect, local cells internalize the plasmid DNA and begin producing VEGF-A protein. This localized expression of VEGF stimulates angiogenesis and promotes the recruitment and differentiation of osteogenic cells, thereby accelerating bone tissue regeneration. Nucleostim-VEGF received marketing authorization in Russia in 2019 following successful Phase III clinical trials, representing a novel intersection of medical devices and gene therapy.

Brand names
Nucleostim-VEGF
Other names
Nucleostim VEGFGistograftHistograft
02

Targets

HSPG (Basement membrane-specific heparan sulfate proteoglycan core protein (perlecan))VEGFR2 (Vascular endothelial growth factor receptor 2)NRP1 (Neuropilin-1)

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