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SIG-018 is a preclinical investigational therapy from Sigilon Therapeutics being developed for mucopolysaccharidosis type II and related congenital and nervous system manifestations associated with iduronate-2-sulfatase deficiency. Based on the provided context, it is described as an iduronate-2-sulfatase modulator intended to address Hunter syndrome biology by acting on the IDS pathway, but no additional public details were provided on its exact molecular format, delivery platform, route of administration, or whether it is designed as direct enzyme replacement, gene-based therapy, or another modality.
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