Catalyst

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Protalix (PLX) has completed a successful Type B Pre-BLA meeting with the FDA regarding the Accelerated Approval pathway for pegunigalsidase alfa (PRX‑102) for the treatment of Fabry disease

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Additional Information

Additional Relevant Details Protalix and Chiesi report that they have reached alignment with the FDA on the Accelerated Approval pathway for pegunigalsidase alfa. The BLA, as expected to be submitted to the FDA, will include data from the Company's completed phase I/II clinical trials of pegunigalsidase alfa and from its ongoing phase III BRIDGE clinical trial.
https://protalixbiot...
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Catalyst Date
Occurred on:
Nov 18, 2019
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Related Keywords Bla Filing, Accelerated Pathway, Pegunigalsidase Alfa, Prx-102, Fabry Disease