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Exhibit 99.1
Tetraphase Pharmaceuticals Reports Fourth Quarter and Full-Year 2016 Financial Results and
Highlights Key 2017 Milestones
Event-Driven 2017 Includes MAA Filing for IV Eravacycline in Europe and Top-Line Data Readout from IGNITE4 in cIAI
Company to Host Conference Call Today, March 8, 2017 at 4:30 p.m. ET
WATERTOWN, Mass., March 8, 2017 Tetraphase Pharmaceuticals, Inc. (NASDAQ:TTPH), a clinical stage biopharmaceutical company developing novel antibiotics to treat life-threatening multidrug-resistant (MDR) infections, today reported financial results for the fourth quarter and year-ended December 31, 2016, highlighted key milestones for 2017 and provided an overview of recent achievements.
2016 marked a year of important progress for Tetraphase as we advanced our phase 3 global development program for IV eravacycline with initiation of IGNITE4 in complicated intra-abdominal infections (cIAI), in which enrollment is proceeding well, and the recent commencement of IGNITE3 in complicated urinary tract infections (cUTI), said Guy Macdonald, President and Chief Executive Officer of Tetraphase. We have laid the groundwork for an event-driven 2017 and look forward to several important IV eravacycline milestones, including the submission of a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) for the treatment of cIAI during the second half of the year and top-line data from IGNITE4 during the fourth quarter, which would support a subsequent NDA filing.
Mr. Macdonald continued, Beyond IV eravacycline, we are also focused on completing the phase 1 clinical development of oral eravacycline and expect to provide an update during the third quarter of 2017, including next steps toward our goal of delivering the first and only IV-to-oral antibiotic transition therapy for the treatment of MDR gram-negative infections.
Key Milestones for 2017
| Submit MAA for IV eravacycline to EMA for the treatment of cIAI 2H 2017 |
| Report top-line data from phase 3 IGNITE4 trial evaluating IV eravacycline in cIAI 4Q 2017 |
| Provide oral eravacycline development program update 3Q 2017 |
| Report phase 1 single-ascending dose data for TP-271 mid-2017 |
| Report phase 1 single-ascending dose data for TP-6076 mid-2017 |
| Initiate phase 1 multiple-ascending dose trials for IV TP-271 and IV TP-6076 2017 |
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