Sobi receives FDA clearance to manufacture Kineret in Austria
Kineret binds to the interleukin-1 type 1 receptor found in various tissues and organs and obstructs the biological activity of IL-1, which is a key mediator of inflammation
The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) Zenbexus (iberdomide), along with daratumumab and hyaluronidase-fihj and dexamethasone (ZDd), to treat adult multiple myeloma (MM) patients.
The Protein Purification Facility will leverage the cGMP compatible stable, non-lytic protein expression platform for expression of complex and challenging proteins, including Fab fragments and other proteins. ExpreS2ion