The Paris-headquartered ERYTECH Pharma S.A. is looking to submit eryaspase to the US Food and Drug Administration in the fourth quarter for hypersensitive acute lymphoblastic leukemia (ALL). This represents a turnaround for the company which had originally filed the product for ALL in the EU before pulling the submission three years ago after deciding that solid tumors, particularly pancreatic cancer, represented the best way forward for the compound. (Also see "Erytech Pulls Graspa ALL Filing To Focus On Pancreatic Cancer" - Scrip, 25 June, 2018.)
Indeed, progress in pancreatic cancer is still on track, and this indication remains the primary focus for the product. Eryaspase...






