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Veglin is an investigational antisense oligonucleotide designed to inhibit the production of vascular endothelial growth factors (VEGF), which are proteins essential for angiogenesis—the formation of new blood vessels. By binding to DNA sequences responsible for encoding VEGF proteins, Veglin blocks their synthesis and thereby restricts the blood supply necessary for tumor growth and metastasis. Developed by VasGene Therapeutics in collaboration with researchers at the University of Southern California, Veglin was intended as a non-chemotherapy anti-angiogenic therapy for various malignancies including mesothelioma, Kaposi's sarcoma, renal cancer, and other solid tumors. Its mechanism involves antagonism of multiple vascular endothelial growth factor receptors (VEGFR-1/2/3). Clinical trials demonstrated some efficacy in reducing or stabilizing tumor burden; however, development has been discontinued across all indications[1][2][3][4][7].
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