Bayer Biological Products Bayer HealthCare - Boliogical Products Division
                SearchSitemap 
HomeAbout UsAbout HaemophiliaFor KidsResearch & DevelopmentPress Releases 
Related Links
   Haemo-QoL Project
   Hemophilia Research Awards
   Living With Hemophilia
   More Haemophila Websites
Bayer Links
   Bayer Global
   Bayer HealthCare
   Bayer BP Global
   Bayer EU Sites
   General Conditions of Use
Privacy Statement
Imprint

© 2004 Bayer HealthCare, LLC

This website is intended for EU residents.

 

Press Releases

Printable Version

Bayer Pursues Divestiture of Plasma Business - Kogenate Business Not Included as Part of Initiative

 
back to Press Releases
October 2, 2003

Leverkusen/Germany. Bayer AG today announced that it is initiating a process to divest its plasma business which is part of the Biological Products (BP) division. The Kogenate line of products and hemophilia franchise is not included as part of this initiative. Bayer BP division will continue to pursue new technologies and maintain reliable supplies of safe products. "Our technology expertise, exciting product line, demonstrated safety expertise, and product pipeline will allow us to continue to provide reliable, high-quality products and services to extend and improve patients' lives" said Dr. Gunnar Riemann, President, Bayer Biological Products . "Our deep pipeline of new products, together with our solid market presence with Prolastin for alpha-1 antitrypsin deficiency and Gamunex and Gamimune N for immune disorders, allows us to work from a position of strength as we pursue this process."

The plasma business recorded sales of EUR 679 million in 2002; sales in the first half of 2003 reached EUR 293 million. The unit, which is headquartered in Research Triangle Park, North Carolina, United States, employs around 1,350 people, the vast majority of them in the U.S.

The range of biological products derived from blood plasma includes drugs such as Polyglobin/Gamimune for the treatment of immunodeficiency disorders and Prolastin for the therapy of congenital pulmonary emphysema.

In August 2003, Bayer was granted marketing authorization in the U.S. for Gamunex, a next-generation intravenous immunoglobulin which had also received regulatory approval in Canada shortly beforehand. This new drug from Bayer Biological Products is the first immunoglobulin in the past ten years to be developed completely from scratch. Gamunex is manufactured in a new, state-of-the-art facility in Clayton, North Carolina.

Forward-Looking Statements
This news release contains forward-looking statements based on current assumptions and forecasts made by Bayer Group management. Various known and unknown risks, uncertainties, and other factors could lead to material differences between the actual future results, financial situation, development or performance of the company, and the estimates given here. These factors include those discussed in our public reports filed with the Frankfurt Stock Exchange and with the U.S. Securities and Exchange Commission (including our Form 20-F). The company assumes no liability whatsoever to update these forward-looking statements or to conform them to future events or developments.

Contact:

For further Information please contact
Dr. Michael Diehl
Bayer HealthCare AG
Leverkusen
Phone: ++49-214-30-58532
Fax: ++49-214-30-71640
e-mail: michael.diehl.md@bayer-ag.de