Population Pharmacokinetic Analyses for Omadacycline Using Phase 1 and 3 Data

Author:

Lakota Elizabeth A.1,Van Wart Scott A.1,Trang Michael1,Tzanis Evan2,Bhavnani Sujata M.1,Safir M. Courtney1,Friedrich Lawrence2,Steenbergen Judith N.2,Ambrose Paul G.1,Rubino Christopher M.1

Affiliation:

1. Institute for Clinical Pharmacodynamics, Inc., Schenectady, New York, USA

2. Paratek Pharmaceuticals, King of Prussia, Pennsylvania, USA

Abstract

Omadacycline, a novel aminomethylcycline antibiotic with activity against Gram-positive and -negative organisms, including tetracycline-resistant pathogens, received FDA approval in October 2018 for the treatment of patients with acute bacterial skin and skin structure infections (ABSSSI) and community-acquired bacterial pneumonia (CABP). A previously developed population pharmacokinetic (PK) model based on phase 1 intravenous and oral PK data was refined using data from infected patients. Data from 10 phase 1 studies used to develop the previous model were pooled with data from three additional phase 1 studies, a phase 1b uncomplicated urinary tract infection study, one phase 3 CABP study, and two phase 3 ABSSSI studies.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

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