ReFacto®
The Newest Member of Our Hemophilia Franchise That Includes:
The First Recombinant Human Factor VIII Albumin-free Formulation
Launched in Europe Mid-1999
Approved in U.S. Spring 2000 for the Control and Prevention of Bleeding in Hemophilia Patients; Launched January 2001
Manufacturing Capacity Expansion in St. Louis Expected in Early 2002
ReFacto® AF to Begin Clinical Trials 2H2001
Providing a Higher Level of Safety for the Hemophilia Community