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Fast Track designation highlights high unmet medical need in the treatment of Fabry disease
Data to be presented in an oral presentation and two poster presentations
Oral Presentation of Long Term Results from the Phase I/II Open-Label Extension Trial of PRX-102 for Fabry Disease
Concurrently the Company Completes Private Placement of $10 Million Convertible Notes
Multi-product facility to support the potential manufacturing of both pegunigalsidase alfa and taliglucerase alfa on a commercial scale
The Protalix medicine alidornase alfa is designed to help cystic fibrosis patients clear their lungs by making mucus thin and loose.
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