29 January 2013
TiGenix successfully renews GMP license for stem cell manufacturing facility in Madrid
Leuven (BELGIUM), Madrid (SPAIN) – January 29, 2013 – TiGenix (Euronext Brussels:TIG), a leader in the field of cell therapy, announced today that further to the cGMPinspection by the Spanish health authorities it has successfully renewed its manufacturingauthorization for stem cell products at its manufacturing facility in Madrid, Spain.
“The GMP facility in Madrid performs a vital function within our organization bymanufacturing high-quality, clinical grade allogeneic stem cell products to fuel our keyclinical programs,” said Wilfried Dalemans, CTO of TiGenix. “It is an important steppingstone before we can move to commercial manufacturing at our state-of-the-art, central GMPmanufacturing site in Sittard-Geleen, the Netherlands. Our strong cell therapy manufacturing capabilities place us at the forefront of the cell therapy industry.”
TiGenix NV (Euronext Brussels: TIG) is a leading European cell therapy company with a marketed product for cartilage repair, ChondroCelect®, and a strong pipeline with clinical stage allogeneic adult stem cell programs for the treatment of autoimmune and inflammatory diseases. TiGenix is based out of Leuven (Belgium) and has operations in Madrid (Spain), and Sittard-Geleen (the Netherlands). For more information please visit www.tigenix.com.
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