CSL Behring obtains expanded label approval for Berinert in Europe
Berinert is additionally indicated for the treatment of acute HAE attacks at all body sites in adults and children in Europe. Eligible and trained patients could even self
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.