More options for people with Fabry disease in Europe

9 May 2023

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A new Fabry disease therapy, PRX-102 (pegunigalsidase alfa), has been given marketing authorization by the European Medicines Agency.

Developed by Israel’s Protalix BioTherapeutics (TASE: PLX) and Italian partner Chiesi Farmaceutici, approval for the enzyme replacement therapy was expected after the EMA’s scientific advisors issued a positive decision earlier in the year.

The product will vie with two other therapies in this class which are already available in Europe - Sanofi’s (Euronext: SAN) Fabrazyme (agalsidase beta) and Takeda’s (TYO: 4502) Replagal (agalsidase alfa).

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