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History

2013
  • Cosmo announces approval of Cortiment™ in the Netherlands.
2012
  • Cosmo announces signing of world-wide licensing agreement for CB-03-01 with Medicis.
  • Cosmo announces acceptance of NDA filing by FDA for Uceris® in February.
2011
  • Cosmo announces filing of NDA for Uceris® (Budesonide MMX) in the USA in December.
  • Cosmo announces data for extension study for Budesonide MMX I nthe US.
  • Cosmo announces the additional approval of LIALDA in the U.S. for the maintenance of remission in patients with ulcerative colitis.
  • Cosmo announces filing of MAA for Cortiment® (Budesonide MMX) in the EU in May.
  • Cosmo announces very positive results of the first parts of the phase II clinical trials following the live transmission of Blu-Colonoscopy at the International Meeting for Advanced Gastroenterology Endoscopy at Humanitas Hospital in Milano.
  • Cosmo announces live transmission of Blu-Colonoscopy at the International Meeting for Advanced Gastroenterology Endoscopy at Humanitas Hospital in Milano.
2010
  • Cosmo announces successful results of phase III trials for Budesonide MMX® in the EU.
  • Cosmo announces successful results of phase III trials for Budesonide MMX® in the US.
  • Cosmo announces delisting of BioXell.
  • Cosmo announces final results of its tender offer for BioXell.
  • Cosmo Pharmaceuticals announces preliminary interim result of its tender offer for BioXell.
2009
  • Cosmo's CB-03-01 phase II pilot study in acne demonstrates superiority over Retin A® on 11 December.
  • Cosmo publishes the public tender offer to acquire BioXell on 8 December.
  • Cosmo offers to acquire BioXell on 18 November.
2008
  • Strategic collaboration with Santarus for U.S rights to Budesonide MMX® and Rifamycin MMX® on 15 December.
  • Licensing agreement with Dr. Falk for Rifamycin SV MMX®.
  • Cosmo awarded US patent for use of its MMX® technology.
2007
  • UK Market launch of Mezavant XL® by Shire plc on 05 November.
  • Licensing agreement with Ferring for Budesonide MMX®.
  • US Market launch of Lialda® by Shire plc on 19 March.
  • IPO on the Swiss Stock Exchange (SWX) on 12 March.
2006
  • FDA approval for the manufacturing of tablets to the USA.
  • Completion of 2.000 sq m plant in Lainate, Milan.
2005
  • Completion of first financing round of €20.4 million by Cosmo Holding S.p.A.
  • Lialda®/Mezavant® Supply Agreement with Shire plc.
2004
  • Opening of an R&D laboratory in Catania, Italy.
2001
  • Lialda®/Mezavant® globally out-licensed to Giuliani S.p.A./ Shire plc*.
1999
  • Filing of the first MMX® Multi Matrix technology patent for the controlled release of tablets in the gastro-intestinal tract.
1998
  • Strategic decision to develop novel oral formulations of off-patent pharmaceutical products to generate new patentable applications.
1997
  • Foundation of Cosmo S.p.A. by purchasing contract manufacturing unit in Lainate (Milan) from Parke Davis (now Pfizer Group).
*sublicensed