Lefamulin Receives Approval in Taiwan for Treatment of Community-Acquired Pneumonia
Retrieved on:
Wednesday, September 8, 2021
The anticipated launch timing of XENLETA in Taiwan is undecided.
Key Points:
- The anticipated launch timing of XENLETA in Taiwan is undecided.
- Nabriva Therapeutics is a biopharmaceutical company engaged in the commercialization and development of innovative anti-infective agents to treat serious infections.
- Nabriva Therapeutics received U.S. Food and Drug Administration approval for XENLETA (lefamulin injection, lefamulin tablets), the first systemic pleuromutilin antibiotic for community-acquired bacterial pneumonia (CABP).
- These forward-looking statements should not be relied upon as representing Nabriva Therapeutics views as of any date subsequent to the date of this press release.