The European Commission (EC) has allowed Astellas Pharma and Theravance to market Vibativ (telavancin hydrochloride) to treat adult patients with nosocomial pneumonia, including ventilator-associated pneumonia, known or suspected to be caused by MRSA when other alternatives are not suitable.
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Vibativ is an once-daily injectable lipoglycopeptide antibacterial agent with a dual mechanism of action against Gram-positive bacteria, including resistant pathogens such as methicillin-resistant Staphylococcus aureus (MRSA).
Astellas Pharma Europe president and CEO Ken Jones said the approval of Vibativ can provide European healthcare professionals with a new, effective hospital antibiotic option for patients with hospital-acquired pneumonia caused by MRSA.
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