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Prothena Corporation plc: Prothena Reports First Quarter 2022 Financial Results and Business Highlights

Net cash used in operating and investing activities was $37.4 million in the first quarter; quarter-end cash and restricted cash position was $544.3 millionAdvanced PRX012, a potential best-in-class, subcutaneous

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Prothena Corp (PRTA) Granted FDA Fast Track Designation for PRX012

Prothena Corp (PRTA) Granted FDA Fast Track Designation for PRX012
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Prothena Corporation plc: Prothena Receives FDA Fast Track Designation for PRX012, a Next-Generation Anti-Amyloid Beta Antibody Under Investigation for the Treatment of Alzheimer s Disease

PRX012 is a potential best-in-class, subcutaneous anti-amyloid beta antibody therapy currently in a Phase 1 clinical study for the treatment of Alzheimer's disease DUBLIN, Ireland, April 26, 2022 (GLOBE

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Subcutaneous Anti-Amyloid Beta Antibody Fast Tracked for Alzheimer Disease

The Food and Drug Administration has granted PRX012, an investigational anti-amyloid beta antibody therapy, Fast Track designation for the treatment of Alzheimer disease.

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Prothena : Announces FDA Clearance of IND for PRX012, a Subcutaneous Anti-Amyloid Beta Antibody Under Investigation for the Treatment of Alzheimer s Disease - Form 8-K

Prothena Announces FDA Clearance of IND for PRX012, a Subcutaneous Anti-Amyloid Beta Antibody Under Investigation for the Treatment of Alzheimer s Disease . | March 28, 2022

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