TiGenix to present at the 7th TERMIS-EU Conference in Davos, Switzerland
PRESS RELEASE
TiGenix to present at the 7th TERMIS-EU Conference in Davos, Switzerland
Leuven (BELGIUM) - June 23, 2017, 07:00h CEST - TiGenix NV (Euronext Brussels and NASDAQ: TIG), an advanced biopharmaceutical company focused on exploiting the anti-inflammatory properties of allogeneic, or donor-derived, stem cells to develop novel therapies for serious medical conditions, today announces that Dr. Marie Paule Richard, Chief Medical Officer of TiGenix, will be speaking at the 7th TERMIS-EU Industry Day taking place from June 26-30, 2017 at the Davos Conference Center, Switzerland.
Dr. Richard will give a presentation at an Industry Symposium on June 28 as part of a session entitled, Clinical evaluation road map and clinical development strategies.
During the coming months, representatives of TiGenix will also be attending the following conferences:
PDA-Advanced Therapy Medicinal Products
Date: June
27-28, 2017
Venue: SH Valencia Palace,
Valencia, Spain
Attendee: Dr. Wilfried Dalemans, Chief Technical
Officer, TiGenix NV
European Society of Cardiology (ESC) Congress
Date: August
26-30, 2017
Venue: Fira Gran Via, Barcelona,
Spain
Attendee: Inmaculada Gilaberte Asin, Clinical
Development Director & Manuel Luque, Senior Clinical Project Manager Allo-CSC 01, TiGenix SAU
Annual Symposium of the International Sepsis Forum
Date: 11-13
September, 2017
Venue: Institut Pasteur, Paris,
France
Attendee: Jesus Gonzalez, Clinical Development Director
Cx611, TiGenix SAU
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Congress of the European Shock Society.
Date: 13-15
September, 2017
Venue: Institut Pasteur, Paris,
France
Attendee: Jesus Gonzalez, Clinical Development Director
Cx611, TiGenix SAU
For more information
Claudia D'Augusta
Chief Financial Officer
T: +34 91 804 92 64
About TiGenix
TiGenix NV (Euronext Brussels and NASDAQ: TIG) is an advanced biopharmaceutical company focused on exploiting the anti-inflammatory properties of allogeneic, or donor-derived, stem cells to develop novel therapies for serious medical conditions.
TiGenix lead product, Cx601, has successfully completed a European Phase III clinical trial for the treatment of complex perianal fistulas - a severe, debilitating complication of Crohn's disease. Cx601 has been filed for regulatory approval in Europe and a global Phase III trial intended to support a future U.S. Biologic License Application (BLA) started in 2017. TiGenix has entered into a licensing agreement with Takeda, a global pharmaceutical company active in gastroenterology, under which Takeda acquired the exclusive right to develop and commercialize Cx601 for complex perianal fistulas outside the U.S. TiGenix' second adipose-derived product, Cx611, is undergoing a Phase I/II trial in severe sepsis - a major cause of mortality in the developed world. Finally, AlloCSC-01, targeting acute ischemic heart disease, has demonstrated positive results in a Phase I/II trial in acute myocardial infarction (AMI). TiGenix is headquartered in Leuven (Belgium) and has operations in Madrid (Spain). For more information, please visit http://www.tigenix.com.