Capital Markets Day
Thursday 25th of June, 2026 | 9:00 AM EDT / 15:00 CEST
St. Regis Hotel, New York & Live Webcast
Featuring discussions with key opinion leaders and presentations by Hansa’s management team.
Click Here to Register & AttendThursday 25th of June, 2026 | 9:00 AM EDT / 15:00 CEST
St. Regis Hotel, New York & Live Webcast
Featuring discussions with key opinion leaders and presentations by Hansa’s management team.
Click Here to Register & AttendCEO’s comments
An oversubscribed rights issue has enabled an offensive investment in project IdeS and has allowed us to retain the pace of development in project anti-alpha-11 and HMD-301. In cooperation with a contract manufacturing organization, we have brought our internally-developed production process to full scale for the fermentation, purification and quality control of the drug candidate, IdeS. The upscaling work has developed positively and we have now produced a first batch of IdeS with high yield and high purity. This batch will be primarily be used for pre-clinical toxicity and safety studies. These studies have been initiated and we plan to have them completed during the spring of 2011. If the outcome of these studies is positive, we will initiate Phase I at the end of 2011 or at the beginning of 2012.
Within project anti-alpha-11, a number of promising antibodies have been identified and the patent portfolio has been consolidated. We have entered a license agreement with Human Genome Sciences Inc. regarding anti-alpha-11 antibodies, and a strong patent position for the anti-alpha-11 program and upcoming pharmaceutical products, has been established.
Our collaboration with Axis-Shield plc has developed successfully. Using Hansa Medical’s prototype assay (HMD-301) for quantifying HBP in plasma, Axis-Shield has developed an optimized version. The registration based trials with this optimized assay will commence at the beginning of 2011. In January 2011, Axis-Shield entered an option agreement with Bio-Rad Laboratories regarding HBP as bio-marker for severe sepsis. This option agreement confirms the potential of this exciting product candidate, as well as strengthening the possibilities of reaching the global market.
These are exciting times for Hansa Medical. During the next 12 months, our plan is to initiate introductory clinical studies with IdeS, to achieve the registration of HMD-301 and to identify an anti-alpha-11 drug candidate suitable for clinical development. Emanuel Björne, CEO of Hansa Medical (publ).
For further information, please contact:
Emanuel Björne, CEO
Tel: +46 707 17 54 77
E-mail: [email protected]
Bo Håkansson, Chairman of the Board of Directors
Tel: +46 705 98 57 22
E-mail: [email protected]