Nabriva Therapeutics
Nabriva Therapeutics Employees
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Christopher Naftzger
Interim CEO, General Counsel and Corporate Secretary
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Nabriva Therapeutics Company Information
Nabriva Therapeutics operates as a commercial-stage biopharmaceutical entity primarily engaged in the development and commercialization of novel anti-infective agents to combat serious infections. The company’s flagship product, XENLETA® (lefamulin), has been approved by the FDA for oral and IV use in treating community-acquired pneumonia (CAP) and by the European Medicines Agency on July 28, 2020. Additionally, Nabriva offers a Named Patient Program that allows healthcare professionals in select countries where XENLETA® is not available to access the drug. The company is also developing CONTEPO™ (fosfomycin for injection), aimed to be a first-in-class epoxide antibiotic in the U.S. for treating complicated urinary tract infections, including acute pyelonephritis. Despite submitting a New Drug Application for CONTEPO™, the FDA issued a Complete Response Letter due to travel restrictions preventing onsite inspections. Nabriva Therapeutics maintains operations in the United States, Austria, and Ireland and actively seeks collaboration and licensing opportunities to expand its portfolio and address infectious diseases globally.