European approval for Xenleta in community-acquired pneumonia
Infectious diseases specialist Nabriva Therapeutics (Nasdaq: NBRV) has won European approval for Xenleta (lefamulin), for the treatment of community-acquired pneumonia (CAP) in adults.
The approval covers use where it is considered inappropriate to use antibacterials that are commonly recommended as a first-line therapy, or when these agents have failed. The US regulator granted approval in August 2019.
Nabriva, which was spun out from Sandoz in 2006, is focused on the pleuromutilins - a type of antibacterial first discovered in the 1950s.
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