UK-based multinational pharmaceutical company Hikma Pharmaceuticals plc (LSE: HIK) (NASDAQ Dubai: HIK) (OTC: HKMPY) announced on Monday that it has introduced the first-of-its-kind, ready-to-use vancomycin premix with room-temperature stability under the brand name TYZAVAN (vancomycin injection, USP) in the United States.
TYZAVAN is offered in pre-filled ready-to-use bags designed to help hospitals, pharmacists, doctors, and nurses treat patients faster, more easily, and with reduced risk.
TYZAVAN, a glycopeptide antibacterial, is indicated for the treatment of infections such as septicaemia; infective endocarditis; skin and skin structure infections; bone infections; and lower respiratory tract infections.
According to Hikma, TYZAVAN is the only FDA-approved vancomycin injection available for adults and paediatric patients (aged one month and older) that can be stored at room temperature and used immediately, eliminating the need for compounding, thawing, assembly or activation to streamline preparation and accelerate treatment.
Amgen's UPLIZNA receives US FDA approval
FDA grants priority review to Bristol Myers Squibb's Opdivo regimen for advanced Hodgkin lymphoma
Zydus Lifesciences enters licence and supply partnership with Formycon
Cereno Scientific's Phase IIb trial of CS1 in PAH approved by US FDA
ALR Technologies announces GluCurve Pet CGM relaunch in Canada
Mirum Pharmaceuticals to acquire Bluejay Therapeutics for HDV treatment
PureTech clears key FDA milestone for Phase 3 development of deupirfenidone
J & D Pharmaceuticals' investigational therapy for HCC receives US FDA Orphan Drug Designation
FDA lifts partial clinical hold on Vanda Pharmaceuticals' tradipitant for motion sickness
TransThera publishes clinical results from US-based Phase 2 trial of tinengotinib in CCA
Hope Medicine wins FDA Fast Track Designation for HMI-115 in endometriosis
MED-EL cochlear implant FDA approved for children 7 months and older
Bayer launches Phase IIa trial of BAY 3401016 for Alport Syndrome