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Name
- Omiganan (MBI-226/MX-226/CLS001)
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Description
- Omiganan (MBI-226), an analogue of indolicidin, has been proven to be capable of significantly reducing catheter colonization and microbiologically confirmed tunnel infections during catheterization
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Target Organism
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- [Ref.19524411]Omiganan was most active against staphylococci, with MICs of 2–4, 2–8, 4 and 4 μg/mL against MSSA, MRSA, MSSE and MRSE strains, respectively. The peptide was also inhibitory against other organisms, with MICs of 8–16 μg/mL against E. coli, E. faecalis and E. faecium (including VSE and VRE strains), 128 μg/mL against E. cloacae and S. marcescens and 64 μg/mL against C. albicans.
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Reference
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- Antimicrobial and antifungal activities of a novel cationic antimicrobial peptide, omiganan, in experimental skin colonisation models.(PMID: 19524411)
- New therapies for atopic dermatitis: Additional treatment classes.(PMID: 29248520)
- Designing antimicrobial peptides: form follows function.(PMID: 22173434)
- Cationic antimicrobial peptides in clinical development, with special focus on thanatin and heliomicin.(PMID: 21964560)
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Medical use
- Rosacea, Acne vulgaris (II), Genital warts (II)
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Company
- Maruho Co., Ltd(developing), Cutanea Life Sciences, Inc.(developing), Mallinckrodt, Micrologix Biotech(Vancouver, BC, Canada)
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Stage of Development
- Phase III(catheter-related infections,Failure), Phase III(rosacea, completed), Phase II(atopic dermatitis (AD), usual type vulval intraepithelial neoplasia (uVIN), external genital warts, and acne vulgaris, completed), Phase III(facial seborrheic dermatitis, recruiting)
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- MX-594AN significantly reduced acne lesions compared with vehicle controls in a phase IIb trial in 2003 and was licensed to Cutanea Life Sciences in late 2005.
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Clinical Trials
- NCT02576847
- NCT03091426
- NCT01784133
- NCT00608959
- NCT00231153