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Chiesi Global Rare Diseases and Protalix BioTherapeutics Announce European Commission Approval of Additional Dosing Regimen of Every Four Weeks for Elfabrio® (pegunigalsidase alfa)
Protalix BioTherapeutics, Inc. (DE) (PLX)
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Source: GlobeNewswire
NASDAQ:AMEX Investor Relations: phx.corporate-ir.net/phoenix.zhtml?c=101161&p=irol-irhome
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This press release is intended for US audiences for transparency relative to global news for the Fabry community. This dosing regimen for Elfabrio is not approved in the
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