Eravacycline, a newly approved fluorocycline
Complicated intra-abdominal infections (cIAIs) are commonly associated with multimicroorganisms and treatment choices are becoming narrower due to developing resistance, especially in the gram-negative Enterobacteriaceae species. Eravacycline is a newly developed, fully synthetic tetracycline deriva...
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Published in: | European journal of clinical microbiology & infectious diseases 2019-10, Vol.38 (10), p.1787-1794 |
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Main Authors: | , |
Format: | Article |
Language: | eng |
Subjects: | |
Online Access: | Get full text |
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Summary: | Complicated intra-abdominal infections (cIAIs) are commonly associated with multimicroorganisms and treatment choices are becoming narrower due to developing resistance, especially in the gram-negative
Enterobacteriaceae
species. Eravacycline is a newly developed, fully synthetic tetracycline derivative that has shown potent broad-spectrum activity against a wide variety of microorganisms, including those such as extended spectrum β-lactamase producing
Enterobacteriaceae
and
Acinetobacter
. Eravacycline has shown activity against many gram-positive organisms such as methicillin-resistant
S. aureus
and vancomycin resistant
Enterococcus faecalis
and
Enterococcus faecium
(VRE), gram-negative organisms such as
Escherichia coli
, and anaerobic species of microorganisms such as
Bacteroides
. This fluorocycline has been compared to ertapenem and meropenem for the treatment of complicated intra-abdominal infections and levofloxacin for the treatment of complicated urinary tract infections. Eravacycline was shown to be noninferior to ertapenem but did not meet noninferiority criteria in comparison to levofloxacin. Oral and IV formulations on eravacycline were tested in clinical trials, but at this time, only the IV formulation is FDA approved. Eravacycline has been noted to have a half-life of 20 h with protein binding around 80%; AUC over minimum inhibitory concentration (MIC) has also been shown to be eravacycline’s best predictor of efficacy. Of note, eravacycline does not require any renal dose adjustments, as the majority of its clearance is by nonrenal pathways. |
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ISSN: | 0934-9723 1435-4373 |