HealthSport, Cure Pharmaceutical sign LOI
Under the non-binding LOI, the parties will contribute technology, research and development and other resources and will negotiate the formation of a joint venture, for the development and
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.