Drug intelligence / Profile preview

AAV-BI30-CBS

Development stage
Preclinical
Lead developer
Beijing Tiantan Hospital
Modality
Gene Therapies
Administration
Intravenous
01

Overview

AAV-BI30-CBS is an investigational gene therapy designed to treat atherosclerosis by reversing endothelial cell senescence. It utilizes the engineered adeno-associated virus serotype 9 (AAV9) variant capsid, AAV-BI30, which has high tropism for endothelial cells, to deliver the gene encoding cystathionine β-synthase (CBS). In preclinical models of atherosclerosis, systemic administration of AAV-BI30-CBS has been shown to alleviate atherosclerotic plaque formation, reduce senescent cell burden in lesions, promote endothelial cell proliferation and autophagy, and inhibit the secretion of the senescence-associated secretory phenotype (SASP).

Other names
AAV-BI30-Cystathionine beta-synthaseAAV-BI-30-Cystathionine beta-synthaseAAV-BI 30-Cystathionine beta-synthaseAAV-BI30-Cystathionine β-synthase

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