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Monday, September 8, 2014

European Medicines Agency accepts TiGenix Paediatric Investigation Plan for Cx601

TiGenix NV , an advanced biopharmaceutical company focused on developing and commercialising novel therapeutics from its proprietary platform of allogeneic, expanded adipose-derived stem cells, or eASC's, in inflammatory and autoimmune diseases, announced today that the Paediatric Committee of the European Medicines Agency has issued a positive opinion on the Company's Paediatric Investigation Plan for Cx601, a locally injected stem cell product in Phase III of clinical development for the treatment of complex perianal fistulas in patients with Crohn's disease. An accepted PIP is a requirement for the filing for marketing authorisation of a new medicinal product with the EMA.

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