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Murepavadin activity tested against contemporary (2016–17) clinical isolates of XDR Pseudomonas aeruginosa
Author(s) -
Hélio S. Sader,
Robert K. Flamm,
Glenn E. Dale,
Paul R. Rhomberg,
Mariana Castanheira
Publication year - 2018
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dky227
Subject(s) - colistin , broth microdilution , microbiology and biotechnology , antimicrobial , pseudomonas aeruginosa , tobramycin , cephalosporin , antibiotics , polymyxin , medicine , biology , minimum inhibitory concentration , bacteria , gentamicin , genetics
Murepavadin (POL7080) represents the first member of a novel class of outer membrane protein-targeting antibiotics. Murepavadin acts by binding to LPS transport protein D and is being developed for the treatment of hospital-acquired and ventilator-associated pneumonia caused by Pseudomonas aeruginosa.

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