The Food and Drug Administration (FDA) approved Carvykti (ciltacabtageneautoleucel; cilta-cel) for the treatment of patients with released or refractory multiple myeloma. The approval is for ...
A March 28 Facebook post (direct link, archive link) includes two images of raw chicken ... the product as "beyond slimy." The post was shared more than 15,000 times in one week. Lab-grown meat ...
Due to adcomm panel meet, the FDA pushed the approval date for Abecma from 16 December 2023. Abecma helped extend the time before disease progression by 13.3 months vs. 4 months in standard care ...
Enhertu has been approved by the FDA for certain patients with unresectable or metastatic HER2-positive solid tumors. The Food and Drug Administration has granted Enhertu (fam-trastuzumab ...
96 shots in 41 seconds: Seatbelt violation leads to death of Black Chicago motorist Common over-the-counter medicine linked to increased dementia risk Boeing 737 Max diverts to Idaho after in ...
Fast Track and Qualified Infectious Disease Product designations for the CABP, ABSSSI and SAB indications. Peter Kim, director of the Division of Anti-Infectives in the FDA's Center for Drug ...
Zevtera is a cephalosporin antibacterial with in vitro activity against gram-positive and gram-negative bacteria, including methicillin-resistant and susceptible Staphylococcus aureus. The Food ...
opens new tab antibiotic for bacterial infections including multidrug-resistant strains, the FDA said on Wednesday. The Switzerland-based company was seeking approval of its antibiotic ...
The Sepsis ImmunoScore was approved through the agency’s De Novo pathway, the process the FDA uses for novel medical devices. Poole said the company plans to sell the Sepsis ImmunoScore at ...
Officials say more research is needed and these findings are just preliminary. Also, FDA approval does not guarantee insurance coverage. It’s still unclear if most insurance companies will cover ...
Vanda Pharmaceuticals (NASDAQ:VNDA) shares jumped 29% premarket on Wednesday after the U.S. Food and Drug Administration (FDA) cleared its Fanapt (iloperidone) tablets for the acute treatment of ...