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Study · In vitro (cells) · pseudomonas aeruginosa · 2018

7 results

Murepavadin activity tested against contemporary (2016-17) clinical isolates of XDR Pseudomonas aeruginosa.

Sader HS, Flamm RK, Dale GE, Rhomberg PR, Castanheira M

The Journal of antimicrobial chemotherapy1 Sept 2018Cited by 47 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study7

7 results from studies that gave the peptide. No result from this study comes from people.

  1. 01LabIn vitro (cells)Activity measurement

    In XDR clinical isolates, murepavadin MIC50/90 was 0.12/0.25 mg/L.

    In plain wordsIn lab tests, murepavadin MIC50/90 was 0.12/0.25 mg/L in XDR isolates.

    Outcome
    Not applicableMIC50 and MIC90
    Study

    Pseudomonas aeruginosan = 785

    XDR clinical isolates
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Measurements

    MIC50
    0.12 mg/L
    Not specified
    MIC90
    0.25 mg/L
    Not specified

    Source sentences

    Summary
    Murepavadin (MIC50/90, 0.12/0.25 mg/L) inhibited 96.7% of isolates at ≤0.5 mg/L and was 8-fold more active than colistin (MIC50/90, 1/2 mg/L).
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.
  2. 02LabIn vitro (cells)Activity measurement

    In XDR clinical isolates, murepavadin inhibited 96.7% at ≤0.5 mg/L.

    In plain wordsIn lab tests, murepavadin inhibited 96.7% of XDR isolates at ≤0.5 mg/L.

    Outcome
    Not applicableIsolate inhibition
    Study

    Pseudomonas aeruginosan = 785

    XDR clinical isolates
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Measurements

    Isolates inhibited
    96.7%
    ≤0.5 mg/L

    Source sentences

    Summary
    Murepavadin (MIC50/90, 0.12/0.25 mg/L) inhibited 96.7% of isolates at ≤0.5 mg/L and was 8-fold more active than colistin (MIC50/90, 1/2 mg/L).
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.
  3. 03LabIn vitro (cells)Activity measurement

    In XDR clinical isolates, murepavadin was 8-fold more active than colistin.

    In plain wordsIn lab tests, murepavadin was 8-fold more active than colistin in XDR isolates.

    Outcome
    IncreaseActivity versus colistin
    Study

    Pseudomonas aeruginosan = 785

    XDR clinical isolates
    Comparator
    Colistin
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Murepavadin (MIC50/90, 0.12/0.25 mg/L) inhibited 96.7% of isolates at ≤0.5 mg/L and was 8-fold more active than colistin (MIC50/90, 1/2 mg/L).
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.
  4. 04LabIn vitro (cells)Activity measurement

    In XDR clinical isolates, seven isolates (0.9%) had murepavadin MIC values above 4 mg/L.

    In plain wordsIn lab tests, seven XDR isolates (0.9%) had murepavadin MIC values above 4 mg/L.

    Outcome
    Not applicableElevated MIC frequency
    Study

    Pseudomonas aeruginosan = 785

    XDR clinical isolates
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Only seven isolates (0.9%) exhibited murepavadin MIC values >4 mg/L.
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.
  5. 05LabIn vitro (cells)Activity measurement

    In tobramycin-non-susceptible XDR isolates, murepavadin MIC50/90 was 0.12/0.25 mg/L.

    In plain wordsIn lab tests, murepavadin MIC50/90 was 0.12/0.25 mg/L in tobramycin-non-susceptible isolates.

    Outcome
    Not applicableActivity in tobramycin-non-susceptible isolates
    Study

    Pseudomonas aeruginosan = 412

    Tobramycin-non-susceptible XDR isolates
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Measurements

    MIC50
    0.12 mg/L
    Not specified
    MIC90
    0.25 mg/L
    Not specified

    Source sentences

    Summary
    Murepavadin remained active against isolates that were non-susceptible to colistin (n = 50; MIC50/90, 0.25/0.25 mg/L), ceftolozane/tazobactam (n = 231; MIC50/90, 0.12/0.25 mg/L) and/or tobramycin (n = 412; MIC50/90, 0.12/0.25 mg/L).
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.
  6. 06LabIn vitro (cells)Activity measurement

    In ceftolozane/tazobactam-non-susceptible XDR isolates, murepavadin MIC50/90 was 0.12/0.25 mg/L.

    In plain wordsIn lab tests, murepavadin MIC50/90 was 0.12/0.25 mg/L in ceftolozane/tazobactam-non-susceptible isolates.

    Outcome
    Not applicableActivity in ceftolozane/tazobactam-non-susceptible isolates
    Study

    Pseudomonas aeruginosan = 231

    Ceftolozane/tazobactam-non-susceptible XDR isolates
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Measurements

    MIC50
    0.12 mg/L
    Not specified
    MIC90
    0.25 mg/L
    Not specified

    Source sentences

    Summary
    Murepavadin remained active against isolates that were non-susceptible to colistin (n = 50; MIC50/90, 0.25/0.25 mg/L), ceftolozane/tazobactam (n = 231; MIC50/90, 0.12/0.25 mg/L) and/or tobramycin (n = 412; MIC50/90, 0.12/0.25 mg/L).
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.
  7. 07LabIn vitro (cells)Activity measurement

    In colistin-non-susceptible XDR isolates, murepavadin MIC50/90 was 0.25/0.25 mg/L.

    In plain wordsIn lab tests, murepavadin MIC50/90 was 0.25/0.25 mg/L in colistin-non-susceptible isolates.

    Outcome
    Not applicableActivity in colistin-non-susceptible isolates
    Study

    Pseudomonas aeruginosan = 50

    Colistin-non-susceptible XDR isolates
    Outcome group
    Infection and antimicrobial activity · Infection
    Studied dose
    Dose not stated

    Measurements

    MIC50
    0.25 mg/L
    Not specified
    MIC90
    0.25 mg/L
    Not specified

    Source sentences

    Summary
    Murepavadin remained active against isolates that were non-susceptible to colistin (n = 50; MIC50/90, 0.25/0.25 mg/L), ceftolozane/tazobactam (n = 231; MIC50/90, 0.12/0.25 mg/L) and/or tobramycin (n = 412; MIC50/90, 0.12/0.25 mg/L).
    1 context sentence
    Summary · context
    Susceptibility testing was performed by the reference broth microdilution method and EUCAST and CLSI interpretative criteria were applied.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    27 Oct 2026, 18:20 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:32 UTC

    First added · source update from Europe PMC

Subjects

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