US20170258816A1 - Antibacterial Use of Halogenated Salicylanilides - Google Patents

Antibacterial Use of Halogenated Salicylanilides Download PDF

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US20170258816A1
US20170258816A1 US15/510,304 US201515510304A US2017258816A1 US 20170258816 A1 US20170258816 A1 US 20170258816A1 US 201515510304 A US201515510304 A US 201515510304A US 2017258816 A1 US2017258816 A1 US 2017258816A1
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mrsa
positive bacteria
niclosamide
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Emilie Flora Aurore DELAVENNE
Daniel Jean Jacques SIMON
Morten Otto Alexander SOMMER
Rasmus Vendler TOFT-KEHLER
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Union Therapeutics AS
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/60—Salicylic acid; Derivatives thereof
    • A61K31/609—Amides, e.g. salicylamide
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0043—Nose
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents

Definitions

  • the invention relates to the halogenated salicylanilides closantel, rafoxanide, oxyclozanide or niclosamide and derivatives thereof including salts, hydrates, esters for use in the topical treatment or prevention of conditions caused by Gram positive bacteria such as Staphylococcus , in particular Staphylococcus aureus , and Streptococcus , in particular Streptococcus pyogenes .
  • the halogenated salicylanilides have a surprisingly low frequency of appearance of resistant mutants in said strains compared to commonly used topical antibiotics.
  • topical formulations comprising a halogenated salicylanilide.
  • MRSA methicillin-resistant Staphylococcus aureus
  • Streptococcus pyogenes Several bacteria have become particularly prominent in recent years and have garnered substantial media attention, especially methicillin-resistant Staphylococcus aureus (“MRSA”) and Streptococcus pyogenes . MRSA infections on the skin and in the airways are common in hospital settings and the broad spectrum resistance of the bacteria to almost all classes of antibiotics (e.g. methicillin, fusidic acid and mupirocin) make it particularly difficult to combat. MRSA infections in patients who have not recently been in hospital (so called community acquired MRSA infections) are becoming increasingly frequent.
  • Fusidic acid is an antibiotic derived from Fusidium coccineum that has been used for over 35 years to treat infections with Staphylococcus aureus .
  • fusidic acid is prescribed for skin infections caused by Staphylococcus aureus .
  • Such infections include impetigo, angular cheilitis (an infection around the mouth), and infected dermatitis. It works by stopping the growth of the bacteria causing the infection.
  • Fusidic acid resistance in S. aureus can be readily selected for by in vitro exposure to the antibiotic, leading to the recommendation that for systemic therapy fusidic acid should only be given in combination with another agent. More controversial is the use of topical fusidic acid in the treatment of cutaneous and soft tissue infections.
  • Increasing fusidic acid resistance in Staphylococcus aureus might be important for three reasons. First, it might mean that systemic fusidic acid can no longer be used in situations where it is clinically indicated. Second, failure of topical treatment may occur, especially in primary care settings where treatment is often empiric. Third, resistance to fusidic acid might be linked to other antibiotic resistances, therefore favoring spread of multiply antibiotic resistant Staphylococcus aureus such as MRSA (methicillin-resistant S aureus ).
  • MRSA methicillin-resistant S aureus
  • Mupirocin is a topical antibiotic used to treat superficial skin infections and to control the spread of methicillin-resistant Staphylococcus aureus (MRSA). Mupirocin resistance was observed shortly after it became available. Prevalence of mupirocin resistance among MRSA isolates has been described mostly in hospitalized adult and elderly patients with wide variability, ranging from 0 to 65% of isolates. Rates of resistance have been shown to correlate with increased use in closed inpatient settings. Very restrictive mupirocin prescriptions for local treatment are now recommended.
  • Impetigo is a highly contagious bacterial infection of the superficial layers of the epidermis. Impetigo is one of the most common skin diseases among children, accounting for about 10% of skin diseases treated in US paediatric clinics.
  • the bacteria typically considered to be responsible are Staphylococcus aureus and Streptococcus pyogenes , and often a combination of the two. Impetigo is usually transmitted by direct contact but fomites also play an important role.
  • Methicillin-resistant Staphylococcus aureus (MRSA) is being found with increasing frequency as a causative bacteria of impetigo.
  • Impetigo has three common clinical varieties: impetigo contagiosa (common impetigo), bullous impetigo, and ecthyma. Features of all three types of impetigo, however, may coexist in any individual patient.
  • Topical compositions containing pharmaceutically active ingredients are known for the treatment of impetigo.
  • Topical mupirocin 2% (Bactroban ointment and cream) is a treatment option, as are older treatments, such as topical gentian violet and vioform.
  • mupirocin is a viable treatment option for MRSA, however, resistance of bacteria to mupirocin has been widely reported.
  • Topical fusidic acid 2% (Fucidin cream) is used for treatment of impetigo, and is thought to be equally as effective as mupirocin.
  • the utility of fusidic acid for treatment of impetigo is limited by the problem of resistance development, as discussed above.
  • Fusidic acid-resistant Staphylococcus aureus has been identified as a causative bacteria in outbreaks of impetigo and its emergence has been associated with increased use of topical fusidic acid. Accordingly, utility of fusidic acid as first-line agent for the treatment of impetigo is questionable due to current resistance levels in the target bacteria.
  • Rumblemulin 1% (Altabax ointment), recently approved by the FDA, is a drug in the new class of pleuromutilin antibiotics for the topical treatment of impetigo due to Staphylococcus aureus (methicillin-susceptible only) or Streptococcus pyogene.
  • a wound is an injury to the body (as from violence, accident, or surgery) that typically involves laceration or breaking of a membrane (as the skin) and usually damage to underlying tissues (Merriam Webster Dictionary). Burns are injuries to tissues caused by heat, friction, electricity, radiation, or chemicals. Wounds and burns are often colonized by microbiologic pathogens, including Gram-positive bacteria, such as Staphylococcus aureus and/or Streptococcus pyogenes ; and Gram-negative bacteria, e.g. Pseudomonas aeruginosa.
  • Mupirocin Bacillroban
  • GSK GSK-Serolidiol
  • Emerging resistance to mupirocin is becoming a concern. In coagulase-negative staphylococci isolates, mupirocin resistance rates are higher, ranging from 12.7% in Europe to 38.8% in the United States.
  • Rumblemulin (Altabax, GSK) is another topical antibiotic used for wound treatment.
  • Fucidin (LEO Pharma) is also effective in primary and secondary skin infections caused by sensitive strains of Staphylococcus aureus, Streptococcus species and Corynebacterium minutissimum.
  • Bacterial infections are a leading cause of death worldwide, and bacterial resistance is greatly reducing available treatment options. There is therefore a need for new antibiotics, for which development of resistance is not widespread in the target bacteria, for the prevention and treatment of topical infections caused or contributed to Gram-positive bacteria such as Staphylococcus aureus and Streptococcus pyogenes is strongly warranted.
  • halogenated salicylanilides are a series of compounds generally used as anthelmintic agents.
  • One such compound is niclosamide (5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenz-amide; also known as 2′,5-dichloro-4′-nitrosalicylanilide, 2-hydroxy-5-chloro-N-(2-chloro-4-nitrophenyl)-benzamide, 5-chloro-2′-chloro-4′-nitrosalicylanilide or 5-chloro-N-(2-chloro-4-nitrophenyl)-salicyl amide):
  • Niclosamide is currently used in humans as an anthelmintic drug to treat intestinal infections and displays overall low toxicity, it is poorly soluble in water, shows low intestinal absorption, and once in the bloodstream, it is quickly cleared via the urinary tract or by enzymatic metabolism in the liver. Therapeutically it is useful against cestoda in humans.
  • Niclosamide has also been shown to prevent the penetration of Schistosoma mansoni through the human skin. As well as used as an anticancer drug, pesticide and as an anti- trypanosoma drug. Virtually all applications and proposed applications of niclosamide target eukaryotic organisms.
  • Niclosamide has also been shown to inhibit viral replication in human cells. However, the mechanism is believed to be through targeting human host cells to provide conditions that prevent the viral life rather than specifically targeting the virus. Accordingly, the viral application of niclosamide result from its ability to target an eukaryotic process.
  • Niclosamide is commercially available in a number of formulations including, but not limited to Bayer73®, Bayer2353®, Bayer25648®, Bayluscid®, Baylucide®, Cestocid®, Clonitralid, Dichlosale®, Fenasal®, HL 24470, Iomesan®, Iomezan®, Manosil®, Nasemo®, Niclosamid®, Phenasal®, Tredemine®, Sulqui®, Vermitid®, Vermitin® and Yomesan®.
  • Niclosamide has been proposed as a possible systemic treatment for chronic lung infections caused by the proteobacterium Pseudo - monas aeruginosa and the actinobacterium Mycoplasmum tuberculosis .
  • Niclosamide has been shown to reduce the quorum sensing response as well as the production of quorum sensing metabolites in P. aeruginosa . Since quorum sensing is considered an important process for the pathogenicity during chronic lung infections caused by this bacterium, it led to proposal that niclosamide could be used as an adjuvant therapy for these infections.
  • Niclosamide does not affect the growth of P. aeruginosa and accordingly does not have any direct antibacterial activity. The concentration required for optimal activity was 20 ⁇ M, however, some inhibition was detected at 1 ⁇ M. (F. Imperi et al., Antimicrobial, Agents and Chemotherapy, 557(2), 996-1005 (2013)).
  • M. J. Macielag et al. tested the antibacterial activity of closantel and related derivatives against the drug-resistant organisms, methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus faecium (VREF) (J. Med. Chem., 41(16), 2939-45 (1998)) but nowhere mentioned the problem with resistance development.
  • MRSA methicillin-resistant Staphylococcus aureus
  • VREF vancomycin-resistant Enterococcus faecium
  • WO 2008/155535 describes the use of halogenated salicylanilides for the treatment of acne, wherein propionibacteria is the bacteria causing the acne. There is no mention of the problem with resistance development.
  • halogenated salicylanilide for the treatment of an infection caused by Gram positive bacteria.
  • the topical use of the halogenated salicylanilides according to the invention have a substantially reduced frequency of spontaneous resistant mutants compared to commonly used topical antibiotics.
  • a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters for use in topical prevention or treatment of an infection or disease caused by Gram positive bacteria, wherein the Gram positive bacteria is not a propionibacteria.
  • the invention thus provides a method of treating a disease or infection caused by Gram positive bacteria in a subject, the method comprising topically administering to the subject an effective amount of a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters; wherein the Gram positive bacteria is not a propionibacteria.
  • a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters
  • a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters for use in the topical prevention or treatment of an infection or disease by Gram-positive bacteria which is resistant to a drug selected from fusidic acid, mupirocin and rumblemulin.
  • the invention thus provides a method of treating or preventing a disease or infection caused by Gram positive bacteria in a subject, the method comprising topically administering to the subject an effective amount of a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters; wherein the Gram-positive bacteria which is resistant to a drug selected from fusidic acid, mupirocin and rumblemulin.
  • a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters
  • a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters for use in topical prevention or treatment of an infection or disease for which fusidic acid, mupirocin or rumblemulin was an approved treatment in Europe on 12 Sep. 2014; wherein the disease or infection is caused by Gram positive bacteria.
  • the invention may provide A method of treating or preventing a disease or infection caused by Gram positive bacteria in a subject, the method comprising topically administering to the subject an effective amount a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters; wherein the infection or disease is an infection or disease for which fusidic acid, mupirocin or rumblemulin was an approved treatment in the US on 12 Sep. 2014; and wherein the disease or infection is caused by Gram positive bacteria.
  • a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters
  • halogenated salicylanilides closantel, rafoxanide, oxyclozanide, or niclosamide or a pharmaceutically acceptable derivative thereof are highly effective against Gram-positive bacteria, such as Staphylococcus aureus and Streptococcus pyogenes and unexpectedly are also very effective in reducing the development of resistance bacteria, such as those mentioned above.
  • the compounds are expected to be very useful topical agents for use in the prevention and/or treatment of diseases or infections.
  • One specific halogenated salicylanilide is niclosamide.
  • Examples of diseases which may be treated by topical administration of the halogenated salicylanilide include impetigo, bacterial conjunctivitis, atopic dermatitis related infections, nasal eradication, sycosis barbae, superficial folliculitis, paronychia erythrasma, secondary infected dermatoses, carbuncles, furonculosis (ecthyma, cellulitis, erysipelas, necrotising fasciitis, secondary skin infections of wounds, dermatitis, scabies, diabetic ulcers and the like).
  • the active ingredient is niclosamide or a derivative thereof or as a hydrate thereof such as niclosamide monohydrate, or salt thereof such as its ethanolamine salt, or piperazine salt or other suitable salts or hydrates of such salts.
  • Niclosamide is bacteriostatic for S. aureus (See FIG. 1 ), i.e. it prevents the growth, but does not kill the bacterium. Surprisingly, niclosamide has been found to have equally good effect on S. aureus strains resistant to methicillin, fusidic acid and mupirocin as non-resistant strains (See FIG. 2 ). Biological testing (inter alia) has also unexpectedly revealed that the halogenated salicylanilides, and particularly niclosamide have lower mutation rate against MRSA 01 than compounds like fusidic acid, mupirocin and rumblemulin (see Table 4).
  • niclosamide analogs can act in a manner similar to niclosamide.
  • Illustrative niclosamide analogs include, but are not limited to closantel (CAS #: 57808-65-8), oxyclozanide (CAS #: 2277-92-1), rafoxanide (CAS #: 22662-39-1), clioxanide (CAS #: 14437-41-3).
  • Suitable niclosamide analogs include brotianide (CAS #: 23233-88-7), 4′-chloro-3-nitrosalicylanilide, 4′-chloro-5-nitrosalicylanilide, 2′-chloro-5′-methoxy-3-nitrosalicyl-anilide, 2′-methoxy-3,4′-di-nitrosalicyl-anilide, 2′,4′-dimethyl-3-nitrosalicylanilide, 2′-ethyl-3-nitrosalicylanilide, 2′-bromo-3-nitrosalicyl-anilide, and the like (EP2049137).
  • niclosamide analogs are intended to be illustrative and not limiting, Methods of making niclosamide analogs are well known to those of skill in the art (see, e.g. WO 2004/006906), which is herein incorporated by reference for all purposes.
  • halogenated salicylanilide is selected from closantel, rafoxanide, oxyclozanide, niclosamide, clioxanide, brotianide, 4′-chloro-3-nitrosalicylanilide, 4′-chloro-5-nitrosalicylanilide, 2′-chloro-5′-methoxy-3-nitrosalicyl-anilide, 2′-methoxy-3,4′-di-nitrosalicyl-anilide, 2′,4′-dimethyl-3-nitrosalicylanilide, 2′-chloro-3,4′-dinitrosalicylanilide, 2′-ethyl-3-nitrosalicylanilide and 2′-bromo-3-nitrosalicyl-anilide, or a pharmaceutically acceptable salt or solvate thereof.
  • halogenated salicylanilide is selected from closantel, rafoxanide, oxyclozanide and niclosamide, or a pharmaceutically acceptable salt or solvate thereof.
  • halogenated salicylanilide is selected from closantel, rafoxanide and oxyclozanide, or a pharmaceutically acceptable salt or solvate thereof.
  • the halogenated salicylanilide is niclosamide, or a pharmaceutically acceptable salt or solvate thereof. It may be that the halogenated salicylanilide is niclosamide in the free-base form of the compound. It may be that the halogenated salicylanilide is a pharmaceutically acceptable salt of niclosamide.
  • a topical pharmaceutical formulation comprising a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters, wherein the components of the formulation are selected such that it provides a local pH of less than 6 at the site of infection.
  • halogenated salicylanilides e.g. niclosamide
  • the formulation does not comprise a buffer or pH modifier. This can mean that the formulation does not significantly alter the naturally low pH of the skin at the site of infection.
  • halogenated salicylanilide e.g. niclosamide
  • halogenated salicylanilides are typically mildly acidic, comprising as they do phenolic groups. Salts of halogenated salicylanilides are typically formed with amines (e.g. ethanolamine) which can provide an increase in local pH.
  • Bacterial decolonisation may be an effective strategy for reducing the incidence of nosocomial (hospital acquired) infections, particularly those associated with MRSA. Many people carry MRSA without symptoms. Decolonising such patients may be beneficial in the prevention of the spread of MRSA in a hospital environment or to reduce the risk of the patient developing an infection following a surgical or medical procedure in hospital.
  • a method of treating, preventing or eliminating bacterial colonization by Gram positive bacteria in a subject comprising topically administering to the subject an effective amount a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters.
  • the invention may provide a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters, for use in treating, preventing or eliminating bacterial colonization in a subject by Gram positive bacteria by topical administration.
  • the halogenated salicylanilide is topically administered to the subject prior to performing a surgical procedure on the subject. It may be that the halogenated salicylanilide is administered to the nose of the subject, either intranasally or to the external skin of the nose. Thus it may be that the halogenated salicylanilide is topically administered to the nose of the subject to performing a surgical procedure on the nose or face of the subject.
  • the Gram-positive bacteria develops spontaneous mutations which confer resistance to the halogenated salicylanilide at a frequency of less than 10 ⁇ 6 at the minimum inhibitory concentration (MIC) of the halogenated salicylanilide to the Gram positive bacteria. It may be that the Gram-positive bacteria develops spontaneous mutations which confer resistance to the halogenated salicylanilide at a frequency of less than 10 ⁇ 7 at the MIC of the halogenated salicylanilide to the Gram positive bacteria. It may be that the Gram-positive bacteria develops spontaneous mutations which confer resistance to the halogenated salicylanilide at a frequency of less than 10 ⁇ 8 at the MIC of the halogenated salicylanilide to the Gram positive bacteria.
  • MIC minimum inhibitory concentration
  • the Gram-positive bacteria develops spontaneous mutations which confer resistance to the halogenated salicylanilide at a frequency of less than 4 ⁇ 10 ⁇ 9 at the MIC of the halogenated salicylanilide to the Gram positive bacteria.
  • the Gram positive bacteria is not a propionibacteria. It may be that the Gram positive bacteria is selected from Staphylococcus aureus or Streptococcus pyogenes . It may be that the bacteria is resistant to a drug selected from fusidic acid, mupirocin and rumblemulin. It may be that the bacteria is methicillin-resistant Staphylococcus aureus (MRSA).
  • MRSA methicillin-resistant Staphylococcus aureus
  • the infection or disease is selected from the group consisting of impetigo, bacterial conjunctivitis, atopic dermatitis and related infections, infected eczema, rosacea, nasal eradication, sycosis barbae, superficial folliculitis, paronychia erythrasma, secondary infected dermatoses, carbuncles, furonculosis, ecthyma, cellulitis, erysipelas, necrotising fasciitis, secondary skin infections of wounds, dermatitis, scabies and diabetic ulcers.
  • the infection or disease is selected from the group consisting of impetigo, bacterial conjunctivitis and atopic dermatitis. It may be that the infection or disease is selected from the group consisting of impetigo, bacterial conjunctivitis, atopic dermatitis related infections, nasal eradication, sycosis barbae, superficial folliculitis, paronychia erythrasma, secondary infected dermatoses, carbuncles and furonculosis (ecthyma, cellulitis, erysipelas, necrotising fasciitis, secondary skin infections of wounds, dermatitis, scabies, diabetic ulcers and the like).
  • the infection or disease is not acne vulgaris.
  • the treatment is administered topically for 2 weeks or less.
  • the halogenated salicylanilide is comprised in a formulation the components of which are selected such that it provides a local pH of less than 6 at the site of infection.
  • the inventors have found that the antibacterial activity of halogenated salicylanilides, e.g. niclosamide, is higher at low pH than at neutral or basic pH. Thus, it may be that the formulation does not comprise a buffer or pH modifier. Thus, it may be that the halogenated salicylanilide, e.g. niclosamide, is in the form of a free base.
  • the components of the formulation may be selected such that it provides a local pH of greater than 4.5 (e.g. greater than 5) at the site of infection. Reference to a “local pH” is to the pH at the site where the formulation is applied for example the pH on the surface of the skin after applying the formulation containing the halogenated salicylanilide.
  • halogenated salicylanilide is selected from rafoxanide, oxyclozanide, closantel and niclosamide and derivatives thereof including salts, hydrates and esters. It may be that halogenated salicylanilide is selected from rafoxanide, oxyclozanide and niclosamide and derivatives thereof including salts, hydrates and esters. Thus, it may be that the halogenated salicylanilide is niclosamide or a salt or hydrate thereof.
  • the halogenated salicylanilide e.g. rafoxanide, oxyclozanide, closantel or niclosamide
  • the halogenated salicylanilide is in the form of a free base. It may be that the halogenated salicylanilide (e.g. rafoxanide, oxyclozanide, closantel or niclosamide) is not in the form of a hydrate. Where the halogenated salicylanilide is niclosamide it may be that it is not in the form of the monohydrate.
  • the Gram-positive bacteria is not an antibiotic resistant strain. Alternatively, it may be that the Gram-positive bacteria is an antibiotic resistant strain.
  • the infection or disease is in a human or animal, for example wherein the infection is in a human.
  • the population of Gram-positive bacteria includes antibiotic-resistant Gram-positive bacteria.
  • the Gram positive bacteria is not a propionibacteria, e.g. that it is not Propionibacterium acnes.
  • the population of Gram-positive bacteria includes coccus gram-positive bacteria.
  • the Gram-positive bacteria are from the Streptococcus or Staphylococcus genus.
  • the Gram-positive bacteria are from the Streptococcus genus. It may be that the Gram-positive bacteria are Streptococcus selected from Streptococcus pneumoniae, Streptococcus pyogenes, Streptococcus suis, Streptococcus agalactiae or Streptococcus viridans.
  • the Gram-positive bacteria are Streptococcus pyogenes
  • the Gram-positive bacteria are from the Staphylococcus genus. It may be that the Gram-positive bacteria are Staphylococcus selected from Staphylococcus epidermidis, Staphylococcus aureus, Staphylococcus saprophyticus or Staphylococcus lugdunensis . In some embodiments, the coccus Gram-positive bacteria are Staphylococcus aureus (e.g. methicillin-resistant Staphylococcus aureus ).
  • the Gram-positive bacteria described herein may be resistant to another antibiotic drug.
  • the bacteria may be resistant to another antibiotic drug other than a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and or niclosamide, or a derivative thereof. It may be that the bacteria is resistant to a drug selected from fusidic acid, mupirocin and rumblemulin.
  • Also provided are methods of treating a subject having a Gram-positive bacterial infection that include topically administering to a subject having a Gram-positive bacterial infection one of the halogenated salicylanilides closantel, rafoxanide, oxyclozanide, or niclosamide or a derivative thereof in amounts sufficient to decrease the population of Gram-positive bacteria in the subject.
  • the invention may be and characterized by a rate of developing spontaneous resistance to these bacteria of less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • One example which is of special interest is niclosamide.
  • the present invention provides a method of treating a subject suffering from an infection contributed to or caused by Gram-positive bacteria as hereinbefore described, said method comprising the step of topically administering an effective amount of a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide, or a derivative thereof.
  • the invention may be characterized by a rate of developing spontaneous resistance to these bacteria of less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • niclosamide which may be characterized by a rate of developing spontaneous resistance to these bacteria of less than 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • the present invention may provide the use of a pharmaceutically effective amount of a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a derivative thereof in the preparation of a medicament for use in the topical prevention and/or treatment of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis.
  • a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis.
  • the invention may be characterized by a rate of developing spontaneous resistance to these bacteria of less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • a rate of developing spontaneous resistance to these bacteria of less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • One example which is of special interest is niclosamide.
  • the present invention may provide a method for the topical prevention and/or treatment of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis comprising administering to a subject a pharmaceutically effective amount of a halogenate salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a hydrate or a salt or a hydrate of such a salt thereof.
  • the invention may be characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • One example which is of special interest is niclosamide.
  • the present invention may provide a method for the topical treatment of antibiotic-resistant Gram-positive bacterial infections comprising administering to a subject infected with antibiotic-resistant Gram-positive bacteria selected from the group consisting of antibiotic-resistant Staphylococcus aureus and/or Streptococcus pyogenes , a pharmaceutically effective amount of a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a hydrate or a salt or a hydrate of such a salt thereof.
  • antibiotic-resistant Gram-positive bacteria selected from the group consisting of antibiotic-resistant Staphylococcus aureus and/or Streptococcus pyogenes
  • a pharmaceutically effective amount of a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a hydrate or a salt or a hydrate of such a salt thereof.
  • the present invention may provide a method for the prevention and/or treatment of conjunctivitis and keratitis caused by Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes comprising topically administering to a subject a pharmaceutically effective amount of a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a hydrate or a salt or hydrate of such a salt thereof.
  • a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a hydrate or a salt or hydrate of such a salt thereof.
  • niclosamide is one example which is of special interest.
  • the present invention may provide a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically effective amount of a halogenated salicylanilide selected from closantel, rafoxanide, oxyclozanide and niclosamide or a derivative thereof to be administered for the topical prevention and/or treatment of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis and characterized by a rate of developing spontaneous resistance to these bacteria of less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczem
  • the present invention may provide a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically effective amount of niclosamide or a derivative thereof to be administered for the topical prevention and/or treatment of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis and characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • the present invention may provide a pharmaceutical composition comprising niclosamide as the active ingredient to be administered for the topical prevention and/or treatment of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis and characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis and
  • diseases which may be topically treated using the halogenated salicylanilide include impetigo, bacterial conjunctivitis, atopic dermatitis related infections, nasal eradication, sycosis barbae, superficial folliculitis, paronychia erythrasma, secondary infected dermatoses, carbuncles, furonculosis (ecthyma, cellulitis, erysipelas, necrotising fasciitis, secondary skin infections of wounds, dermatitis, scabies, diabetic ulcers and the like).
  • the infection or disease treated topically using the halogenated salicylanilide may be a skin infection, infected dermatitis or infected dermatosis, for example any of the skin infections described herein.
  • the skin infection may, for example, be selected from impetigo (including impetigo contagiosa, bullous impetigo, and ecthyma) infected dermatitis (for example infected atopic dermatitis) infected eczema, infected skin wounds, infected burns and infected ulcers (for example diabetic ulcers).
  • the infection or disease treated topically using the halogenated salicylanilide may be a secondarily Gram positive infected dermatosis, for example a secondary skin infection.
  • Secondary Gram positive infections are common complications of primary dermatoses, primary nonbacterial skin infections, traumatic lesions, ulcers, cutaneous infestations, and other skin diseases.
  • the halogenated salicylanilide may be for use in the topical treatment of for example secondary infections of a condition selected from eczema, pediculosis, scabies, insect bites (for example papular urticaria), pemphigus psoriasis, skin ulcers, kerion and a viral infection of the skin (for example herpes simplex or chicken pox).
  • the halogenated salicylanilide may be for use to decolonise a subject carrying a Gram positive bacteria (including any of the Gram positive bacteria described herein, for example MRSA), wherein the halogenated salicylanilide is applied topically to the subject.
  • a Gram positive bacteria including any of the Gram positive bacteria described herein, for example MRSA
  • Such decolonisation may be effective in preventing or reducing the spread of infection to other subjects particularly in a hospital environment. Decolonisation may also prevent or reduce the risk of surgical site infections resulting from surgical or medical procedures carried out on the patient or at the site of medical devices such as catheters or IV lines or cannula.
  • the halogenated salicylanilide may be for use in the decolonisation of a subject prior to carrying out a surgical procedure on the subject, wherein the halogenated salicylanilide is applied topically to the subject.
  • Such surgical procedures include, for example elective surgical procedures such as hip or knee replacement.
  • Decolonisation may be achieved by topically administering the halogenated salicylanilide to sites on the subject which are colonised by the Gram positive bacteria. It is known that a common site for bacterial colonisation such as MRSA is the nose. Accordingly, the halogenated salicylanilide may be applied topically to the nose. Particularly the halogenated salicylanilide may be applied to the anterior nares (the inner surface of the nostrils).
  • infections and decolonisation described in the above paragraphs and herein may be topically treated with any of the halogenated salicylanilides herein selected from closantel, rafoxanide, oxyclozanide or niclosamide or a derivative thereof.
  • the halogenated salicylanilide may be niclosamide.
  • the present invention may provide a pharmaceutical composition
  • a pharmaceutical composition comprising a pharmaceutically effective amount of one of the halogenated salicylanilides closantel, rafoxanide, oxyclozanideor niclosamide or a derivative thereof to be administered for the topical prevention and/or treatment of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes colonizing or infecting skin affected with a dermatological condition selected from the group consisting of impetigo, atopic dermatitis and infections associated with different skin conditions such as eczema or psoriasis characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 against MRSA 01, MRSA 15 and MRSA 16 at a concentration of MIC ⁇ 1 when measured according to mutational frequency evaluation method as described in the experimental section.
  • Niclosamide has been found to be
  • a further aspect of the invention also provides a halogenated salicylanilide selected from the group consisting of closantel, rafoxanide, oxyclozanide, and niclosamide and derivatives thereof including salts, hydrates and esters for use in the topical prevention or treatment of an infection caused by Gram-positive bacteria, are highly effective in inhibiting the growth of Gram-positive bacteria such as Staphylococcus , in particular Staphylococcus aureus , and Streptococcus , in particular Streptococcus pyogenes characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • niclosamide is one example which is of special interest.
  • a further aspect of the invention also provides a method for manufacturing of a medicament for use in topical prevention or treatment of an infection caused by Gram-positive bacteria, wherein the medicament is niclosamide and derivatives thereof including salts, hydrates and esters and wherein the use of the halogenated salicylanilide are highly effective in inhibiting the growth of Gram-positive bacteria such as Staphylococcus , in particular Staphylococcus aureus , and Streptococcus , in particular Streptococcus pyogenes characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • Gram-positive bacteria such as Staphylococcus , in particular Staphylococcus aureus
  • Streptococcus in particular Streptococcus pyogenes characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇
  • halogenated salicylanilides such as niclosamide it is possible to treat a human suffering from an infection caused by bacteria such as Staphylococcus aureus or Streptococcus pyogenes while having a reduced rate of appearance of spontaneous resistant mutants against the agent.
  • FIG. 1 shows microbiological data of niclosamide tested against MRSA, MSSA and S. pyogenes strains.
  • the MIC of niclosamide was ⁇ 0.4 ⁇ g/ml against S. aureus strains, including the strains resistant to fusidic acid (*) and the ones resistant to mupirocin (+), and ⁇ 3.2 ⁇ g/ml against Streptococcus pyogenes strains.
  • Dose-response curves of yellow highlighted strains are represented in B.
  • FIG. 2 shows a time-kill curve of MRSA 01 incubated with niclosamide (MIC ⁇ 10).
  • Niclosamide had a bacteriostatic effect against MRSA 01 (strain used in animal experiment) in the tested conditions (initial inoculum: 7 log 10 cfu/ml; niclosamide: 4 ⁇ g/ml [MIC ⁇ 10]).
  • FIG. 3 shows CFU in skin lesions after three days of treatment with Samples 5.
  • Sample-control corresponds to the sample without niclosamide *: P ⁇ 0.05, unpaired t-test; **: P ⁇ 0.005, unpaired t-test; ***: P ⁇ 0.001, unpaired t-test; ns: not significant.
  • FIG. 4 shows the dose-response curves of niclosamide, fusidic acid and mupirocin against S. aureus with methicillin-resistant strains (A), fusidic acid-resistant strain (B) and mupirocin-resistant strain (C).
  • FIG. 5 shows the growth of S. aureus at different pH as a function of niclosamide concentration (average of 3 replicates).
  • the growth of S. aureus without niclosamide (0 ⁇ g/ml) is comparable from pH 7.4 to pH 6.0.
  • the growth without niclosamide is slightly inhibited at pH 5.5 and completely inhibited with pH equal or below 5.0.
  • Staphylococcus aureus or “ S. aureus ” as used herein, without further description, relates to any strain of the gram-positive bacteria classified as Staphylococcus aureus , and which have been associated with a number of infections, including pneumonia, osteomyelitis, arthritis, endocarditis, sepsis and toxic shock syndrome, as well as cause less severe infections of the skin and soft tissues.
  • MRSA methicillin-resistant Staphylococcus aureus
  • strains of Staphylococcus aureus that are resistant to methicillin and can also broadly relate to Gram-positive bacteria strains (e.g. beta-lactamase-producing bacteria) that are resistant to antibiotics falling within the general classification of penicillins.
  • Methicillin is the common name for (2S,5R,6R)-6-[(2,6-dimethoxybenzoyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, which is a narrow spectrum beta-lactam antibiotic that has been used to treat infections caused by susceptible Gram-positive bacteria (e.g. including Staphylococcus aureus ).
  • susceptible Gram-positive bacteria e.g. including Staphylococcus aureus
  • derivative refer to, but shall not be limited to metabolites, pro-drugs (converted into active drugs), esters, hydrates and/or a pharmaceutically acceptable salt and/or hydrates of such salts of the halogenated salicylanilides of the present invention. Also within the term “derivatives” are crystalline forms of the compounds and co-crystals formed between the halogenated salicylanilide and a suitable co-former(s).
  • pharmaceutically acceptable salt refers to salts (e.g. ethanolamine or piperazine salts) that retain the biological effectiveness and properties of the compounds described herein and, which are not biologically or otherwise undesirable.
  • Pharmaceutically acceptable salts are well known to skilled persons in the art. Accordingly, it may be that a reference to a salt of a halogenated salicylanilide herein may refer to a pharmaceutically acceptable salt of the halogenated salicylanilide.
  • solvate is used herein to refer to a complex of solute, such as a compound or salt of the compound, and a solvent. If the solvent is water, the solvate may be termed a hydrate, for example a monohydrate, dihydrate, trihydrate etc., depending on the number of water molecules present per molecule of substrate.
  • treatment indicates (i) the prevention of the disease caused by bacteria, such as Staphylococcus aureus and/or Streptococcus pyogenes ; (ii) the suppression of the disease caused by bacteria, such as Staphylococcus aureus and/or Streptococcus pyogenes ; and (iii) the relief of the disease caused by bacteria, such as Staphylococcus aureus and/or Streptococcus pyogenes ; v) the eradication of a non-symptomatic colonization by Staphylococcus aureus from an area on the body, (v) the eradication of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes symptomatic infection, (vi) the eradication of Gram-positive bacteria such as Staphylococcus aureus and/or Streptococcus pyogenes ; from an area of the body affected
  • treatment of a condition encompasses both therapeutic and prophylactic treatment, of either an infectious or a non-infectious condition, in a mammal such as a human or animal, but in particular a human. It may involve complete or partial eradication of the condition, removal or amelioration of associated symptoms, arresting subsequent development of the condition, and/or prevention of, or reduction of risk of, subsequent occurrence of the condition.
  • the bacterial strain may be characterized by a rate of developing spontaneous mutation frequency less than 10 ⁇ 6 , such as less than 10 ⁇ 7 or 10 ⁇ 8 , such as less than 4 ⁇ 10 ⁇ 9 .
  • the treatment will typically involve the use of the halogenated salicylanilides closantel, rafoxanide, oxyclozanide or niclosamide or derivatives thereof against Gram-positive bacteria such as Staphylococcus aureus and Streptococcus pyogenes .
  • One example which is of special interest is niclosamide.
  • the infection or disease which is to be treated is in an animal, e.g. a mammal.
  • the halogenated salicylanilide can be used to treat commercial animals such as livestock (e.g. cows, sheep, chickens, pigs, geese, ducks, goats, etc.).
  • livestock e.g. cows, sheep, chickens, pigs, geese, ducks, goats, etc.
  • the compounds of the present invention can be used to treat companion animals such as cats, dogs, horses, etc.
  • a “topical medication” is a medication that is applied to body surfaces such as the skin or mucous membranes to treat ailments via a large range of classes including but not limited to creams, foams, gels, droplets, lotions, and ointments. Topical medications differ from many other types of drugs because mishandling them can lead to certain complications in a patient or administrator of the drug. Many topical medications are epicutaneous, meaning that they are applied directly to the skin. Topical medications may also be inhalational, such as asthma medications, or applied to the surface of tissues other than the skin, such as eye drops applied to the conjunctiva, or ear drops placed in the ear, or medications applied to the surface of a tooth.
  • a suitable pharmaceutical composition for example a cream, lotion, gel, ointment, paste, drops or the like, may be spread on the affected surface and gently rubbed in.
  • a solution may be applied in the same way, but more typically will be applied with a dropper, swab, or the like, and carefully applied to the affected areas.
  • Topical application of the halogenated salicylanilide according to the present invention enables the halogenated salicylanilide to be delivered selectively to a specific site, and avoids inter- and intra-patient variations which may be associated with alternative routes of drug administration.
  • Topical pharmaceutical compositions according to the present invention may be used to treat a variety of skin or membrane disorders, such as infections of the skin or membranes (e.g. infections of nasal membranes, axilla, groin, perineum, rectum, dermatitic skin, skin ulcers, and sites of insertion of medical equipment such as i.v. needles, catheters and tracheostomy or feeding tubes) with any of the bacteria described above, (e.g. any of the Staphylococci, Streptococci such as S. aureus (e.g. methicillin resistant S. aureus (MRSA)).
  • infections of the skin or membranes e.g. infections of nasal membranes, axilla, groin, perineum, rectum, dermatitic skin, skin ulcers, and sites of insertion of medical equipment such as i.v. needles, catheters and tracheostomy or feeding tubes
  • any of the bacteria described above e.g. any of the Staphylococci,
  • Particular bacterial conditions that may be treated by topical pharmaceutical compositions of the present invention also include the skin- and membrane-related conditions disclosed hereinbefore, as well as: rosacea (including erythematotelangiectatic rosacea, papulopustular rosacea, phymatous rosacea and ocular rosacea); erysipelas; erythrasma; ecthyma; ecthyma gangrenosum; impetigo; paronychia; cellulitis; folliculitis (including hot tub folliculitis); furunculosis; carbunculosis; staphylococcal scalded skin syndrome; surgical scarlet fever; streptococcal perianal disease; streptococcal toxic shock syndrome; pitted keratolysis; trichomycosis axillaris ; pyoderma; external canal ear infections; green nail syndrome; spirochetes; nec
  • kansasii M. malmoense, M. szulgai, M. simiae, M. gordonae, M. haemophilum, M. avium, M. intracellular, M. chelonae (including M. abscessus ) or M. fortuitum infections, swimming pool (or fish tank) granuloma, lymphadenitis and Buruli ulcer (Bairnsdale ulcer, Searles' ulcer, Kakerifu ulcer or Toro ulcer)); as well as infected eczema, burns, abrasions and skin wounds.
  • Particular fungal conditions that may be treated by topical pharmaceutical compositions of the present invention also include the skin- and membrane-related conditions disclosed hereinbefore, as well as: candidiasis; sporotrichosis; ringworm (e.g. tinea pedis, tinea cruris, tinea capitis, tinea unguium or tinea corporis ); tinea versicolor ; and infections with Trichophyton, Microsporum, Epidermophyton or Pityrosporum ovale fungi.
  • the topical pharmaceutical compositions of the present invention is not used to treat a fungal infection, for example the composition is not used to treat candidiasis; sporotrichosis; ringworm (e.g. tinea pedis, tinea cruris, tinea capitis, tinea unguium or tinea corporis ); tinea versicolor ; and infections with Trichophyton, Microsporunm, Epidermophyton or Pityrosporum ovale fungi.
  • the application regimen will depend on a number of factors that may readily be determined, such as the severity of the condition and its responsiveness to initial treatment, but will normally involve one or more applications per day on an ongoing basis.
  • the effective dosage of the pharmaceutical composition of the present invention varies from the formulation, administration pathway, age, weight and gender of animal or human with a disease caused by Staphylococcus aureus , severity of a disease, diet, administration frequency and pathway, excretion and sensitivity.
  • the amount of the halogenated salicylanilide or a derivative thereof to be administered topically is in the range of 0.01-10000 mg/cm 2 , preferably between 0.1-1000 mg/cm 2 and even more preferably between 1-100 mg/cm 2 using a pharmaceutical formulation containing between 1-20%, preferably 2-10%, more preferably 3-8% and even more preferably 4-6% of active ingredient (all numbers given by weight).
  • minimum inhibitory concentration In microbiology, minimum inhibitory concentration (MIC) is the lowest concentration of an antibacterial that will inhibit the visible growth of a microorganism after overnight incubation. Minimum inhibitory concentrations are important in diagnostic laboratories to confirm resistance of microorganisms to an antimicrobial agent and also to monitor the activity of new antimicrobial agents. A MIC is generally regarded as the most basic laboratory measurement of the activity of an antimicrobial agent against an organism.
  • LD 50 (abbreviation for “lethal dose, 50%”) of a toxin, radiation, or pathogen is the dose required to kill half the members of a tested population after a specified test duration. LD 50 figures are frequently used as a general indicator of a substance's acute toxicity.
  • Therapeutic index is defined as the amount of a therapeutic agent causing the therapeutic effect measured as MIC to the amount that causes death in animal studies measured as LD 50 .
  • Some antibiotics require monitoring to balance efficacy with minimizing adverse effects, including: gentamicin, vancomycin, amphotericin B (nicknamed ‘ampho-terrible’ for this very reason), and polymyxin B. Other MIC values could be used as well.
  • the rate of resistance development is quantified as the frequency of spontaneous mutants in a population of bacteria that is able to resist a given concentration of the antibiotic. For example the rate of resistance development may by 10 ⁇ 9 if on average 1 cell in 10 9 cells is able to survive a concentration of antibiotic corresponding to 1 ⁇ MIC.
  • colony-forming unit is a rough estimate of the number of viable bacteria or fungal cells in a sample. Viable is defined as the ability to multiply via binary fission under the controlled conditions.
  • MRSA 01 strain methicillin-resistant S. aureus 01 strain was used as the primary test microorganism. This strain is a community-acquired MRSA clinical isolate of USA 300 type, from a skin abscess.
  • Strains were conserved in Luria Bertani (LB) Broth ( S. aureus ) or Brain Heart Infusion (BHI) ( S. pyogenes ) supplemented with glycerol 15% (v/v) at ⁇ 80° C., and reactivated by isolation on LB ( S. aureus ) or BHI ( S. pyogenes ) agar plates. Strains were cultivated in Mueller Hinton (MH) Broth-cation adjusted ( S. aureus ) supplemented with lysed horse blood 2.5% (v/v) ( S. pyogenes ). All strains were cultivated at 37° C., aerobically for S. aureus strains.
  • MH Mueller Hinton
  • MRSA 07 All Staphylococcus aureus strains but one (MRSA 07) are human clinical isolates; MRSA 07 is a Livestock-associated MRSA; MRSA 02 and MRS 04 are Community-associated MRSA; * strains resistant to fusidic acid; ⁇ strains resistant to mupirocin; ND: Not determined; EEFIC: Epidemic European Fusidic acid-resistant Impetigo Clone; MLST: Multilocus Sequence Typing; SSCmec: staphylococcal cassette chromosome mec; spa: S. aureus protein A; KU: Copenhagen University; SSI: National Reference Laboratory for Staphylococci, Statens Serum Instityt, Copenhagen, Denmark.
  • the MIC was determined using 96-well plates, and serial two-fold dilutions of niclosamide (from Sigma) (from 51.2 to 0.025 ⁇ g/ml) in above indicated medium, with 150 ⁇ l per well.
  • the inhibition could be either due to a bactericidal or a bacteriostatic activity, which is not known from this experiment.
  • the following assay was thus carried out in order to determine if niclosamide kills or inhibits growth of S. aureus.
  • Assay was performed in 20 ml of medium. It included a negative control (medium without bacteria), a positive control (bacteria grown without niclosamide) and the assay (bacteria grown with niclosamide). Nicolosamide was tested at 10 fold its MIC, determined in the previous experiment. This experiment was performed with the primary test microorganism indicated above.
  • the overnight culture was stopped and OD 600 was measured.
  • Culture was then diluted in indicated medium to obtain an OD 600 of 0.25 in order to have about 5 ⁇ 10 8 cfu/ml.
  • Two hundred ⁇ 1 of this diluted culture were then added in all conditions except in the negative control.
  • Initial bacterial concentration was about 5 ⁇ 10 6 cfu/ml. Tubes were incubated aerobically at 37° C. for 24 hours.
  • Bacteria were enumerated before the incubation, after 30 minutes, 1, 2, 4, 8 and 24 hours of incubation by serial dilutions in NaCl 0.9% and plating on LB agar, with 2 plates per dilution. Plates were incubated at 37° C. and colonies enumerated after 24 hours.
  • the compound was considered bactericidal if the reduction of the bacterial inoculum was superior or equal to 3 log 10 cfu/ml, bacteriostatic if reduction was inferior to 3 log 10 cfu/ml.
  • Viable cell growth was enumerated after 48 hours of incubation at 37° C.
  • CFU Colony-Forming Unit
  • mice received a skin lesion approximately 1 cm 2 and were challenged with 1.5 ⁇ 10 8 cfu MRSA 01 topically. Twenty-four hours after the wound formation and the contamination, mice were treated topically with 0.05 ml twice daily for three days. Mice were sacrificed on day 4, skin lesions were excised and cfu quantitated. Fusidin ointment (2% from Leo Pharma) was included as control.
  • Sample 5 Niclosamide (N) 5% modified basis creme with higher lipid content—Lipocreme—according to the description in danske Laegemiddelsstandarder (DLS).
  • Oil phase Polysorbate 80 10 g Cetostearyl alcohol 100 g Paraffin oil 100 g Glycerol monostearate 40-50 120 g Water phase: Methyl parabenzoate 1 g Glycerol 85% 40 g Sorbitol 70 g Water Milli-Q 724 g
  • halogenated salicylanilides such as closantel, oxyclozanide, rafoxanide and particularly niclosamide are strongly potent against Gram-positive strains such as S. aureus and S. pyogenes .
  • the effect is independent of the resistance profile of the isolates towards other currently used antibiotics for topical treatment of these microorganisms, including fucidic acid and mupirocin.
  • the halogenated salicylanilides in general and niclosamide in particular are well suited as a possible treatment for both susceptible and resistant Gram-positive strains.
  • the mutational frequency data gives the frequency of a resistant mutant within a given population.
  • the mutational frequency is bellow 10 ⁇ 9 means that there is less than one resistant mutant in a population of 10 9 cells.
  • the resistance development towards halogenated salicylanilides in general and niclosamide in particular is much slower than resistance development towards drugs like fusidic acid, mupirocin and rumblemulin being on the market.
  • niclosamide particularly useful for treatment, especially topical treatment of infections caused by Gram positive organisms.
  • niclosamide has very unique properties that make it an ideal candidate as a topical anti-infective animal experiments were performed to test the effect of niclosamide in vivo.
  • MRSA 01 strain methicillin-resistant S. aureus 01 strain was used as the primary test microorganism. This strain is a community-acquired MRSA clinical isolate of USA 300 type, from a skin abscess.
  • Strains were conserved in Luria Bertani (LB) Broth ( S. aureus ) or Brain Heart Infusion (BHI) ( S. pyogenes ) supplemented with glycerol 15% (v/v) at ⁇ 80° C., and reactivated by isolation on LB ( S. aureus ) or BHI ( S. pyogenes ) agar plates. Strains were cultivated in Mueller Hinton (MH) Broth—cation adjusted ( S. aureus ) or BHI ( S. pyogenes ). All strains were cultivated aerobically (microaerobically for S. pyogenes strains) at 37° C.
  • MH Mueller Hinton
  • MICs Minimum inhibitory concentrations (MICs) of niclosamide, fusidic acid, and mupirocin were determined according to CLSI criteria with a doubling dilution concentration range (16 to 0.008 ⁇ g/ml) in Mueller Hinton Broth cation-adjusted (Fluka Analytical 90922), using 96-well plates, for 205 different S. aureus strains.
  • S. aureus ATCC 29213 was included as a control reference strain and clindamycin and vancomycin were included as control antibiotics.
  • niclosamide The MIC of niclosamide was ⁇ 0.5 ⁇ g/ml against all targeted S. aureus and S. pyogenes strains, including the strains resistant to fusidic acid, mupirocin, clindamycin and rumblemulin (Table 5, Table 6, Table 7 and FIG. 4 ).
  • Dose-response curves of niclosamide, fusidic acid and mupirocin against S. aureus with different resistance profiles are represented in Figure X.
  • MIC90, MIC50 and MIC ranges of niclosamide for Staphylococcus aureus strains TABLE 7 MIC90, MIC50 and MIC ranges of niclosamide for Staphylococcus aureus strains.
  • MIC90 MIC50 Range values 0.5 ⁇ g/ml 0.25 ⁇ g/ml 0.125-0.5 ⁇ g/ml
  • Niclosamide was inhibitory at a concentration equal or below 0.5 ⁇ g/ml. for all targeted S. aureus and S. pyogenes strains, including fusidic acid- and mupirocin-resistant strains.
  • MRSA 01, MRSA15 [fusidic acid-resistant strain] and MRSA 16 [mupirocin-resistant strain] were chosen for their relevance regarding bacterial skin infections.
  • MRSA 01 strain was used as the primary test microorganism. This strain is a community-acquired MRSA clinical isolate of USA 300 type, from a skin abscess.
  • Strains were conserved in Luria Bertani (LB) Broth supplemented with glycerol 15% (v/v) at ⁇ 80° C., and reactivated by isolation on LB agar plates. Strains were cultivated aerobically in Mueller Hinton (MH) Broth—cation adjusted at 37° C.
  • LB Luria Bertani
  • MH Mueller Hinton
  • Viable cell growth was enumerated after 48 hours of incubation at 37° C.
  • the spontaneous resistance frequency for an isolate-drug combination was calculated from the number of colonies that grew on plates containing drug versus the number of colonies that grew on drug-free agar.
  • Frequencies of spontaneous mutations conferring resistance to niclosamide in Staphylococcus aureus were much lower than frequencies of spontaneous mutations conferring resistance to fusidic acid, mupirocin and rumblemulin in Staphylococcus aureus . This supports the use of niclosamide for cutaneous decolonization of S. aureus.
  • MRSA 01 strain methicillin-resistant S. aureus 01 strain was used. This strain is a community-acquired MRSA clinical isolate of USA 300 type, from a skin abscess.
  • MICs minimal inhibitory concentrations
  • MRSA 01 grew equally well from pH 6 to pH 7.4 (OD 600 ⁇ 0.2 in average in positive control wells) and slightly less in pH 5.5 (OD 600 ⁇ 0.1 in average in positive control wells). However, the strain was inhibited by the lowest pH (pH 4 to pH 5) ( FIG. 5 ).

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