Protalix Biotherapeutics and Chiesi Global Rare Diseases Provide Regulatory Update on PRX-102 for the Treatment of Fabry Disease
Protalix BioTherapeutics and Chiesi Farmaceutici Announce Receipt of "Agreement Letter" for Initial Pediatric Study Plan for PRX-102 for the Treatment of Fabry Disease
Will Protalix BioTherapeutics Keep Powering Higher After its 178% Run Up Since November 2022? - VectorVest
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Protalix BioTherapeutics Expands Partnership with Chiesi Farmaceutici to Include Exclusive US Rights for the Development and Commercialization of PRX-102 (pegunigalsidase alfa)
Shareholders Unite | Protalix PRX-102: Likely Approval Could Be A Game Changer | TalkMarkets
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FDA Action Alert: Sarepta, Protalix, Otsuka/Lundbeck and More | BioSpace
Protalix BioTherapeutics and Chiesi Global Rare Diseases Announce Submission of Biologics License Application to US Food and Drug Administration for Pegunigalsidase Alfa for the Treatment of Fabry Disease
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Protalix BioTherapeutics Issues 2023 Letter to Stockholders
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Fabry Disease Pipeline and Clinical Trials Assessment (2023)