Founded in 1907, the SIU is comprised of over 4,400 members from over 120 countries around the world. The organization’s mission is to enable urologists in all nations to apply the highest standards of urological care to their patients by supporting urologists in helping communication of scientific information, promoting formal and informal relations between national urological societies, and fostering cooperation between urologists from all around the world. Astellas has been supporting the SIU for many years by sponsoring the “Astellas Award” to recognize outstanding research in the field of urology since 1994.
Astellas established a global leading position in urology through offering a treatment for functional symptoms of benign prostatic hyperplasia known as Harnal® in Japan and Omnic® / Omnic OCAS® in Europe, and a treatment for overactive bladder, Vesicare®. Astellas launched a treatment for overactive bladder with a new mechanism of action, mirabegron (generic name) , in September 2011 in Japan (product name in Japan: Betanis®), and submitted new drug applications for mirabegron in the U.S. and Europe in August 2011.
Astellas will continue supporting the SIU’s efforts to enhance medical care in the field of urology.
* Societe Internationale d’Urologie website:http://www.siu-urology.org/
Astellas Pharma Inc. (Headquarters, Tokyo; President & CEO, Yoshihiko Hatanaka) today announced that the administration of the seasonal influenza HA vaccine ASP7374 (former code: UMN-0502) was successfully completed in the currently ongoing phase I/II clinical trial. Astellas Pharma has been pursuing drug development of this vaccine in cooperation with UMN Pharma Inc. (Headquarters, Akita; CEO, Shu-ichi Kanazashi).
This clinical study enrolled 165 healthy adult volunteers, and aims to comparatively evaluate the immunogenicity and safety of two subcutaneous and one intramuscular doses of ASP7374 to determine the optimal clinical dose.
The seasonal influenza HA vaccine ASP7374, which contains three different strains of antigens, has been produced by the cell-culture manufacturing method employing the Baculovirus Expression Vector System (BEVS), a next-generation technology platform for manufacturing of biopharmaceutical products. In USA, Protein Sciences Corporation has completed all clinical studies required for approval, and submitted a Biologic License Application of this vaccine to the Food and Drug Administration.
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