Ceregene starts enrollment in Parkinson’s study
This trial follows positive results from a phase I trial of the gene therapy CERE-120 in 12 patients in which preliminary data showed the treatment to be well
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.