FDA rejects Eli Lilly appeal
Reuters said that the US drug regulator stood by the approvable letter that it sent Eli Lilly last September, which informed the drugmaker that a further study would
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.