Acadia schizophrenia trial shows promising results
The trial enrolled 423 patients across sites in both the US and Brazil. The primary endpoint of the study was antipsychotic efficacy as measured after day 42 compared
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.
The trial compared Zyvox to vancomycin, oxacillin, or dicloxacillin (comparator antibiotics) in the treatment of seriously ill patients with intravascular catheter-related bloodstream infections including those with catheter-site infections.