NBRV - Nabriva Therapeutics' lefamulin application accepted for review in China
Nabriva Therapeutics (NBRV) announces that its partner, Sumitomo Pharmaceuticals’ new drug application (NDA) to market oral and intravenous (IV) formulations of lefamulin for the treatment of community-acquired pneumonia (CAP) in adults has been accepted for review in China. "This is the 6th global filing for lefamulin. To date there have been 4 approvals and two applications pending review,” said Ted Schroeder, Chief Executive Officer of Nabriva Therapeutics.
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Nabriva Therapeutics' lefamulin application accepted for review in China