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Study shows innovative ERT-based solution has the potential to address unmet clinical needs across a range of lysosomal storage diseases

noviembre 19, 2012

Human Health

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Oxyrane, today announced the publication in Nature Biotechnology, results of its landmark study in novel enzyme replacement therapy (ERT) for lysosomal storage diseases (LSDs). Oxyrane, in collaboration with VIB researchers from Ghent University and Vrije Universiteit Brussels, have developed a new technology that enables a more efficient approach to ERT production for LSD treatments, as well as the potential to significantly improve future treatments for debilitating and often life‐threatening LSDs such as Pompe disease, Fabry disease and Hunter’s syndrome.