Nabriva Therapeutics plc. is hardly the first antibiotics company to experience a disappointing product launch, but the COVID-19 pandemic presented multiple unexpected challenges in the months after the August 2019 approval of the first-in-class, semi-synthetic pleuromutilin antibiotic Xenleta. The company’s initial hospital-based focus in community-acquired bacterial pneumonia (CABP) has been scrapped for a community health system focus.
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