Drug intelligence / Profile preview

ALN-VSP

Development stage
Phase 1
Lead developer
Alnylam Pharmaceuticals
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Intravenous
01

Overview

**ALN-VSP** is an investigational, systemically administered lipid-nanoparticle RNA interference therapeutic developed for liver cancers and advanced solid tumors involving the liver. The product contains two chemically modified small interfering RNAs directed against **vascular endothelial growth factor A** and **kinesin family member 11**, also known as kinesin spindle protein. By inducing RNA interference-mediated degradation of the corresponding messenger RNAs, ALN-VSP is intended to suppress tumor angiogenesis through VEGF-A reduction and inhibit mitosis and tumor-cell proliferation through KIF11 reduction. Alnylam evaluated intravenous ALN-VSP02 in a Phase I study and licensed China, Hong Kong, Macau, and Taiwan development rights to Ascletis, which used the internal designation ASC06.

Other names
anti-KSP/anti-VEGF siRNAs
02

Targets

VEGFA (Vascular endothelial growth factor A)KIF11 (Kinesin Spindle Protein)

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