Research for Arialys Therapeutics Announces U.S. FDA Fast Track Designation for ART5803, the First Precision Therapeutic Candidate in Development for the Treatment of Anti-NMDA Receptor Encephalitis - aVenture Research
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Arialys Therapeutics Announces U.S. FDA Fast Track Designation for ART5803, the First Precision Therapeutic Candidate in Development for the Treatment of Anti-NMDA Receptor Encephalitis
LA JOLLA, Calif.--(BUSINESS WIRE)--#ANRE--Arialys Therapeutics, a clinical-stage biotechnology company pioneering precision medicines for autoimmune neuropsychiatric diseases, today announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation to ART5803 for the treatment of anti-NMDA receptor encephalitis (ANRE). ART5803 is a novel therapeutic candidate designed using structural biology to specifically inhibit the pathogenic effects of autoantibodies that target