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France's Erytech Closer To Realizing Market Ambitions With Eryaspase US Filing

Positive FDA Feedback For Leukemia Submission

 
• By Kevin Grogan

It has taken almost two decades but it looks as though Erytech could get approval for eryaspase in the US in two indications next year – acute lymphoblastic leukemia and pancreatic cancer.

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Erytech sorting submission out for eryaspase • Source: Archive

Founded in 2004, ERYTECH Pharma S.A. is finally closing in on getting a product to market after talks with regulators in the US laid an approval pathway for the French biotech's lead candidate eryaspase.

The Paris-headquartered firm is looking to submit eryaspase, which consists of the enzyme L-asparaginase (L-ASP) that is encapsulated inside donor-derived red blood cells, to the US Food and Drug Administration...

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