Hollis-Eden requests approval of metabolic drug trial
The phase I trial program, designed to assess the safety of the drug candidate HE3286, could support both a phase II study in type 2 diabetes patients, as
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.