Genta enters compassionate use agreement with IDIS
The global agreement covers all territories except the US. Named patient distribution refers to the distribution or sale of a product to a specific healthcare professional for the
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.