USA-based biopharma firm Paratek Pharmaceuticals has announced positive top-line efficacy data for Nuzyra (omadacycline) as post-exposure prophylaxis (PEP) in a non-human primate (NHP) model of inhalational anthrax.
Nuzyra is the company’s lead product and is approved in the USA for the treatment of adults with community-acquired bacterial pneumonia (CABP) and acute bacterial skin and skin structure infections (ABSSSI).
Last June, Paratek entered into a definitive agreement to be acquired by Gurnet Point Capital and Novo Holdings.
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