AOP Orphan reveals positive cystic fibrosis drug data
Moli1901 is being developed by AOP Orphan in Europe under a licensing and commercialization agreement with Lantibio. The study was designed to investigate safety and tolerability of aerosolized
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.