Actavis to acquire Warner Chilcott
The transaction, if successfully completed, is expected to create a global specialty pharmaceutical company with around $11bn in combined annual revenue, and the third-largest US specialty pharmaceutical company
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 partnership will leverage DBV’s skin patch, Viaskin, and Stallergenes’ expertise in respiratory allergies in developing immunotherapy treatments for respiratory allergies. DBV Technologies chairman and CEO Dr. Pierre-Henri