Investor Relations

Overview

Nabriva Therapeutics is a commercial-stage biopharmaceutical company engaged in the development of novel antibiotics to treat serious infections. Nabriva Therapeutics has two products: Xenleta™ (lefamulin), recently approved by the FDA for both Oral and IV use, and CONTEPO (fosfomycin) for injection. We resubmitted an NDA for CONTEPO, a potential first-in-class epoxide antibiotic in the United States for complicated urinary tract infections (cUTIs), including acute pyelonephritis (AP). The FDA has assigned a PDUFA date of June 19,2020 for CONTEPO. Our corporate headquarters are in Dublin, Ireland with offices and labs located in Vienna, Austria and King of Prussia, PA.

Events & Presentations

Upcoming
More events are coming soon.
Prior

Thursday June 4, 2020 1:00 PM EDT
Jefferies Virtual Healthcare Conference

Wednesday May 13, 2020 11:00 AM EDT
BofA Securities 2020 Virtual Health Care Conference

SEC Filings

Filing date Description Form Filing Group View
D
Other
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A preliminary proxy statement providing notification matters to be brought to a vote

PRE 14A
Proxy Filings
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A preliminary proxy statement providing notification matters to be brought to a vote

PRE 14A
Proxy Filings
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Investor Contacts

E-mail: IR@nabriva.com