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Chiesi Fabry disease treatment gets EU marketing authorization

Thread starter cafead
Start date May 10, 2023

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cafead

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cafead May 10, 2023 at 10:22: AM

via Chiesi Global Rare Diseases and Protalix BioTherapeutics, Inc. have announced that the European Commission (EC) has granted marketing authorization to PRX-102 (pegunigalsidase alfa) in the European Union (EU) for the treatment of adult patients with Fabry disease.

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