Paratek Announces Acceptance of European Marketing Authorization Application for Oral and Intravenous Omadacycline

— MAA submission for both community-acquired bacterial pneumonia (CABP) and acute bacterial skin and skin structure infections (ABSSSI) — 

— EMA decision expected second half of 2019 —
BOSTON, Oct. 04, 2018 (GLOBE NEWSWIRE) — Paratek Pharmaceuticals, Inc. (NASDAQ: PRTK) today announced the acceptance of the submission to the European Medicines Agency (EMA) of the Marketing Authorization Application (MAA) for omadacycline.  Paratek is seeking approval of omadacycline, a modernized tetracycline, for the treatment of community-acquired bacterial pneumonia (CABP) and acute bacterial skin and skin structure infections (ABSSSI).  Omadacycline is a once-daily oral and intravenous (IV) bro…

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