TIG
Os dejo las últimas noticias de Tigenix, que no las había colgado
18-3-2016
Notice in relation to the convertible bonds due 2018
Conversion Price for the Bonds has been adjusted downwards, following the placement by the Company announced on March 10, 2016 of 25,000,000 new shares at an issue price of € 0.95 per new share, or € 23,750,000 in total, with cancellation of the preferential subscription rights for the existing shareholders of the Company. As a consequence, the Calculation Agent has determined that the Conversion Price is to be adjusted from its previous level of € 0.9414 to the new level of € 0.9263 per TiGenix share (after rounding in accordance with Condition 6.6 of the Terms and Conditions of the Bonds). The Conversion Price adjustment became effective on March 14, 2016.
17-3-2016
TiGenix Presents 24 Week Results of its Cx601 Phase III Trial at ECCO 2016
a single injection of Cx601 achieved statistically significant superiority vs. placebo in the primary efficacy endpoint of combined remission at week 24 (defined as clinical assessment of closure of all treated external openings draining at baseline, despite gentle finger compression, and absence of collections >2cm confirmed by MRI; p=0.024). This definition of remission is more stringent than those commonly used in clinical trials on perianal fistulizing disease, as it includes both clinical and radiological assessment by MR
https://finance.yahoo.com/news/tigenix-presents-24-week-results-181009458.html#morequotes
10-3-2016
Tigenix raises 23.75 million euros in private placement
25 million shares at an average price of 0.95
7-3-2016
positive 52-week Phase III results of Cx601 in complex perianal fistulas in Crohn's disease patients
2-3-2016
submission of a centralized Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for Cx601 for the treatment of complex perianal fistulas in adult patients with Crohn's diseaseobtained the license for commercial production of Cx601, TiGenix's product for the treatment of complex perianal fistulas in Crohn's disease patients
"This timely and successful achievement fulfils one of the final requirements for our plan to file a Marketing Approval Application for Cx601 at the European Medicines Agency (EMA) in the coming weeks," said Maria Pascual, VP Regulatory Affairs. "In this way our plan remains in line with the expectation to make Cx601 available to European patients in the second half of 2017
https://finance.yahoo.com/news/tigenix-obtains-commercial-production-license-060936709.html
Y, como recordatorio, tiene previsto subir al Nasdaq
«Después de nada, o después de todo/ supe que todo no era más que nada.»