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Liposomal disintegrin is an investigational anti-tumor therapeutic being developed by Molecular Express. It consists of a disintegrin—a potent, non-enzymatic protein typically derived from snake venom—encapsulated within a liposomal delivery vehicle. Disintegrins are characterized by their ability to bind specifically to integrins, such as alpha-V/beta-3 (αvβ3), alpha-V/beta-5 (αvβ5), and alpha-5/beta-1 (α5β1), which are often overexpressed on the surface of many cancer cells and the endothelial cells of tumor-associated blood vessels. By competitively inhibiting these integrins, the drug disrupts cell-extracellular matrix interactions, thereby blocking cell adhesion, migration, and tumor-induced angiogenesis. The liposomal formulation is designed to improve the pharmacokinetics, stability, and targeted delivery of the disintegrin peptide to the tumor microenvironment, potentially reducing systemic toxicity while enhancing efficacy.
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