ERYTECH Granted U.S. FDA Fast Track Designation for Eryaspase in Hypersensitive ALL

On July 29, 2021 ERYTECH Pharma (Nasdaq & Euronext: ERYP), a clinical-stage biopharmaceutical company, leader in red blood-cell based cancer therapeutics, reported that the U.S. Food and Drug Administration (FDA) has granted eryaspase Fast Track designation for the treatment of acute lymphocytic leukemia (ALL) patients who have developed hypersensitivity reactions to E. coli-derived pegylated asparaginase (PEG-ASNase) (Press release, ERYtech Pharma, JUL 29, 2021, View Source [SID1234585452]).

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