Nabriva Therapeutics plc (NASDAQ: NBRV), announced today that its partner, Sumitomo Pharmaceuticals’ (Suzhou) Co., Ltd., new drug application (NDA) to market oral and intravenous (IV) formulations of lefamulin for the treatment of community-acquired pneumonia (CAP) in adults in mainland China has been accepted for review by the Chinese Center for Drug Evaluation (CDE), China’s regulatory authority, on November 23, 2021.
November 29, 2021
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