ERYtech Pharma creates high value products for hospital market, mainly in oncology, hematology and immunology fields.
ERYtech Pharma has a first success with its lead compound Graspa® which demonstrated positive results and excellent safety profile compared to control treatment in Phase II trials in acute lymphoblastic leukaemia. Phase III in leukaemia started in 2009 and a development program of Graspa® in several other indications notably solid tumors is ongoing.

Headquartered in France (Lyon) with a cGMP manufacturing unit, ERYtech Pharma has a US Office and a US location for cGMP clinical batches production at the American Red Cross.

ERYtech Pharma’s business & revenue model is both:
  • An integrated business & revenue model for proprietary product to maximize value creation
  • A business development revenue model based on its R&D platform and partnership
 
Main achievements and highlights:

2010
  • Agreement with M. D. Anderson Cancer Center to develop a companion test for Graspa® in solid tumors
  • FDA grants Orphan Drug Designation to Graspa® for treatment of Acute Lymphoblastic Leukaemia
2009
  • Pivotal Clinical Trial for Graspa® in Acute Lymphoblastic Leukaemia in Europe
  • Phase II Clinical Trial with Graspa® as first-line treatment among patients with Acute Lymphoblastic Leukaemia aged 55 and older
  • cGMP facility certification from the French Health Products Safety Agency (AFSSAPS)
  • American Red Cross manufacturing and supply agreements
  • ISO 9001:2008 certification
  • Granted by the French Ministry of Research
  • Supervisory Board and Scientific Board reinforced
2008
  • Phase I/II Clinical Trial for Graspa® last patient enrolled and results presented at the 50th Annual Meeting of the American Society of Hematology (ASH) in San Francisco
  • Granted by France's National Research Agency and the Lyon Auvergne Rhône-Alpes Cancer Research Cluster (CLARA)
2007
  • Phase I/II Clinical Trial for Graspa®: launching in Belgium
  • New Headquarters, R&D laboratory and cGMP facility in Lyon
2006
  • Phase I/II Clinical Trial for Graspa®: first patient enrolled
  • EMEA awards Medicinal Product classification for Graspa®
  • EMEA awards Orphan Drug Designation for Graspa®
  • Financing round A € 12 million
2005
  • Seed Financing Round € 750.000 with financial shareholders and business angels
  • Granted by the French Ministry of Research, France's National Research Agency, Rhône-Alpes Région and the Lyon Auvergne Rhône-Alpes Cancer Research Cluster (CLARA)
2004
  • ERYtech Pharma incorporation
  • Granted by the French Ministry of Research and award from the Rhône-Alpes Ouest Créalys business incubator

Erytech Pharma
Last Update 01/09/2010
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