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Name
- Murepavadin (POL7080)
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Sequence
- cyclo[Ala-Ser-D-Pro-Pro-Thr-Trp-Ile-Dab-Orn-D-Dab-Dab-Trp-Dab-Dab]
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Description
- synthetic by amino acid substitution of protegrin I.
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Target Organism
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- [Ref.29686157]Murepavadin (MIC50/90, 0.12/0.12 mg/liter) was 4- to 8-fold more active than colistin (MIC50/90, 1/1 mg/liter) and polymyxin B (MIC50/90, 0.5/1 mg/liter) and inhibited 99.1% of isolates at ≤0.5 mg/liter. Only 4 isolates (0.3%) exhibited murepavadin MICs of >2 mg/liter. Murepavadin was equally active against isolates from Europe, the United States, and China.
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Reference
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- Antimicrobial Activity of Murepavadin Tested against Clinical Isolates of Pseudomonas aeruginosa from the United States, Europe, and China.(PMID: 29686157)
- Murepavadin activity tested against contemporary (2016–17) clinical isolates of XDR Pseudomonas aeruginosa.(PMID: 29901750)
- Cyclic peptide therapeutics: past, present and future.(PMID: 28249193)
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Medical use
- Treatment of nosocomial pneumonia and ventilator-associated bacterial pneumonia (VABP)
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Stage of Development
- Phase III(suspended, adverse events)
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- This is a phase 3, multicenter, open-label, sponsor blinded, randomized active-controlled, parallel group to investigate the efficacy, safety and tolerability of intravenous murepavadin given with ertapenem versus an anti-pseudomonal β-lactam based antibiotic in the treatment of nosocomial pneumonia in adult subjects (ClinicalTrials.gov Identifier: NCT03582007). This is a phase 3, multicenter, open-label, randomized active-controlled, parallel group to investigate the efficacy, safety and tolerability, and pharmacokinetics of intravenous murepavadin combined with of one anti-pseudononas antibiotic with that of two anti-pseudomonas antibiotics in the treatment of ventilator-associated bacterial pneumonia (VABP) in adult subjects (ClinicalTrials.gov Identifier: NCT03409679).
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Clinical Trials
- NCT03409679
- NCT03582007
- NCT02096328