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Chiesi Global Rare Diseases Announces Presentations on Lysosomal Storage Diseases at the Society for the Study of Inborn Errors of Metabolism Annual Symposium

Published: September 2, 2022

Results from the clinical development programme developed with Protalix BioTherapeutics evaluating pegunigalsidase alfa (PRX-102) an investigational enzyme...

Source: prnewswire.com

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United StatesUnited KingdomFriuli Venezia GiuliaAlpha MannosidosisEtoile AlphaUma RamaswamiChiesi FarmaceuticiNathalie GuffonGiacomo ChiesiMaurizio ScarpaB CorpGroup ChiesiLisbon North Hospital Center PortugalProtalix LtdBerry Company Public RelationsProtalix BiotherapeuticsChiesi GroupUnited Nations Sustainable Development Goals SdgsRegional Reference CentreRare DiseasesUdine University HospitalGlobal Rare DiseasesInborn ErrorsAnnual SymposiumRoyal Free Hospital