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Chiesi Global Rare Diseases and Protalix BioTherapeutics Announce Validation of Variation Submission by European Medicines Agency for pegunigalsidase alfa
Protalix BioTherapeutics, Inc. (DE) (PLX)
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Source: PR Newswire
NASDAQ:AMEX Investor Relations: phx.corporate-ir.net/phoenix.zhtml?c=101161&p=irol-irhome
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- Application to label a less frequent dosing regimen at a dose of 2 mg/kg body weight administered every four weeks in adult patients with Fabry disease in European Uni
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