SINGLE DOSE METHODS FOR PREVENTING AND TREATING FUNGAL INFECTIONS
20230181689 · 2023-06-15
Inventors
- Kenneth BARTIZAL (La Jolla, CA, US)
- Paul DARUWALA (Del Mar, CA, US)
- Jeffrey B. LOCKE (La Jolla, CA, US)
- Voon ONG (San Diego, CA, US)
- Taylor SANDISON (Encinitas, CA, US)
Cpc classification
A61K9/0019
HUMAN NECESSITIES
A61K9/0053
HUMAN NECESSITIES
A61K38/1774
HUMAN NECESSITIES
A61K38/12
HUMAN NECESSITIES
A61K31/407
HUMAN NECESSITIES
International classification
A61K9/00
HUMAN NECESSITIES
Abstract
Provided herein are methods for treating, mitigating, or preventing fungal infections or related conditions thereto in a human subject in need thereof. The methods include the administration of a single dose of a pharmaceutical composition comprising or consisting of CD101 and any pharmaceutically acceptable excipients, wherein the single dose treatment substantially reduces or eliminates the fungal infection.
Claims
1. A method of treating a C. auris infection in a subject in need thereof comprising administering a pharmaceutical composition comprising CD101 salt, or a neutral form thereof, and one or more pharmaceutically acceptable excipients, to the subject in an amount and for a duration sufficient to treat the C. auris infection.
2. The method of claim 1, wherein the C. auris infection is a drug-resistant C. auris infection.
3. The method of claim 2, wherein the drug-resistant C. auris infection is resistant to treatment with an echinocandin, a polyene, a flucytosine, or an azole.
4. The method of claim 2, wherein the drug-resistant C. auris infection is an echinocandin-resistant C. auris infection, a polyene-resistant C. auris infection, a flucytosine-resistant C. auris infection, or an azole-resistant C. auris infection.
5. The method of claim 4, wherein the C. auris infection is caused by a C. auris having a mutant 1,3-β-D-glucan synthase enzyme complex.
6. The method of claim 5, wherein the C. auris comprises one or more mutations in FKS genes.
7. The method of claim 6, wherein the C. auris comprises an FKS1 mutation.
8. The method of claim 7, wherein the C. auris comprises a mutation in the hot spot 1 (HS1) region of FKS1.
9. The method of claim 1, wherein the administering step comprises administering a single dose of the CD101 salt or neutral form thereof to the subject.
10. The method of claim 9, wherein the CD101 is administered orally, subcutaneously, or intravenously.
11. The method of claim 10, wherein the single dose comprises about 50 mg to about 1200 mg of the CD101 salt or neutral form thereof.
12. The method of claim 9, wherein the administration of the single dose substantially eliminates a fungal infection.
13. The method of claim 1, wherein the subject does not receive any concurrent antifungal treatment.
14. The method of claim 1, wherein the subject does not receive any antifungal treatment within 21 days following the administration of the pharmaceutical composition.
15. The method of claim 1, wherein the pharmaceutical composition consists of the CD101 salt, or a neutral form thereof, and the one or more pharmaceutically acceptable excipients.
16. The method of claim 1, wherein the C. auris infection is candidemia, oropharyngeal candidiasis, esophageal candidiasis, mucosal candidiasis, genital candidiasis, vulvovaginal candidiasis, rectal candidiasis, hepatic candidiasis, renal candidiasis, pulmonary candidiasis, splenic candidiasis, otomycosis, osteomyelitis, septic arthritis, cardiovascular candidiasis, or invasive candidiasis.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION
[0102] Provided herein are methods for treating, mitigating, or preventing a fungal infection or related conditions thereto in a human subject in need thereof. The methods include the administration of a single dose of a pharmaceutical composition including or consisting of CD101 and any pharmaceutically acceptable excipients, wherein the single dose treatment substantially reduces or eliminates the fungal infection.
I. Treatment Applications
[0103] The invention features methods for treating, mitigating, or preventing a fungal infection in a human subject in need thereof, wherein the fungal infection is associated with a disruption in the levels or composition of fungal species (e.g., Candida infection, Aspergillus infection, or Pneumocystis infection) in or on one or more body regions or tissues of the host subject. Further, the method can be used to treat symptoms, manifestations, conditions, or diseases associated with a fungal infection. In some instances, the fungal infection can be a primary diagnosis (e.g., the root cause of a symptom or condition), secondary to another condition or disease (e.g., a symptom or outcome of another condition); or a combination thereof. The fungal infection may be associated with one or more fungal species and/or colonization of the fungal species on one or more body regions or tissues of the host subject.
[0104] The methods of the invention can treat a fungal infection, for example, by reducing colonization by one or more opportunistic or non-opportunistic pathogenic fungi (e.g., by about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or %100 relative to a starting amount) in one or more parts of the body in an amount sufficient to restore a normal fungal population (e.g. approximately the amount found in a healthy individual) and/or allow benefit to the individual (e.g., reducing colonization in an amount sufficient to sustainably resolve symptoms). For example, a fungal infection can be caused by overgrowth of an opportunistic pathogen that is normally present on the human body but has grown above healthy levels, in which case the infection may be eliminated by reducing fungal species to a level typically found in a healthy individual without necessarily eliminating the fungal species. Alternatively, for example, a fungal pathogen or opportunistic pathogen may colonize a portion of the body in which it does not typically reside and thus, the infection is treated when the fungal population is eradicated.
[0105] The methods of the invention can prevent a fungal infection, for example, by preventing an increased colonization by one or more opportunistic or non-opportunistic pathogenic fungi (e.g., prevent increase of about 1%, 2%, 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, %100, or more than %100 relative to a starting amount) in one or more parts of the body in an amount sufficient to maintain a normal fungal population (e.g., approximately the amount found in a healthy individual), prevent the onset of a fungal infection, and/or prevent symptoms or conditions associated with infection. For example, subjects may receive prophylaxis treatment to substantially prevent a fungal infection while being prepared for an invasive medical procedure (e.g., preparing for surgery, such as receiving a transplant, stem cell therapy, a graft, a prosthesis, receiving long-term or frequent intravenous catheterization, or receiving treatment in an intensive care unit), in immunocompromised subjects (e.g., subjects with cancer, with HIV/AIDS, or taking immunosuppressive agents), or in subjects undergoing long term antibiotic therapy.
[0106] In some instances, the methods provided herein can be used to treat a fungal infection associated with, or partially associated with, a fungal infection or fungal overgrowth localized to one or more portions of the human body. In some instances, the fungal species can be any species belonging to the phylum Ascomycota, Basidomycota, Chytridiomycota, Microsporidia, or Zygomycota. The fungal infection or overgrowth can include one or more fungal species, e.g., Candida albicans, C. tropicalis, C. parapsilosis, C. glabrata, C. auris, C. krusei, Saccharomyces cerevisiae, Malassezia globose, M. restricta, or Debaryomyces hansenfi, Gibberella moniliformis, Alternaria brassicicola, Cryptococcus neoformans, Pneumocystis carinii, P. jirovecii, P. murina, P. oryctolagi, P. wakefieldiae, and Aspergillus clavatus. The fungal species may be considered a pathogen or an opportunistic pathogen. Further, the fungal species may be found indigenously in or on the human body (e.g., occurs sustainably regardless of level or concentration) or it can exist transiently in or on the human body.
[0107] In some instances, the fungal infection is caused by a fungus in the genus Candida (i.e., a Candida infection). For example, a Candida infection can be caused by a fungus in the genus Candida that is selected from the group consisting of C. albicans, C. glabrata, C. dubliniensis, C. krusei, C. auris, C. parapsilosis, C. tropicalis, C. orthopsilosis, C. guilliermondii, C. rugose, and C. lusitaniae. Candida infections that can be treated by the methods of the invention include, but are not limited to candidemia, oropharyngeal candidiasis, esophageal candidiasis, mucosal candidiasis, genital candidiasis, vulvovaginal candidiasis, rectal candidiasis, hepatic candidiasis, renal candidiasis, pulmonary candidiasis, splenic candidiasis, otomycosis, osteomyelitis, septic arthritis, cardiovascular candidiasis (e.g., endocarditis), and invasive candidiasis.
[0108] Clinical isolates of C. auris that may be treated or prevented by the methods described herein are described in the Examples section (e.g., Example 7) and also in Lee et al., J Clin Microbiol. 49:3139-42, 2011, Kathuria et al., J Clin Microbiol. 53:1823-30, 2015, and Vallabhaneni et al., MMWR Morb Mortal Wkly Rep. 65:1234-1237, 2016, each of which is incorporated by reference herein in its entirety. For example, FIG. 2 of Kathuria describes clinical isolates of C. auris which are shown in Table 1.
TABLE-US-00001 TABLE 1 # Clinical isolate 1 VPCI 717/P/14 2 VPCI 462/P/14 3 VPCI 1156/P/13 4 VPCI 271/P/14 5 VPCI 471/P/14 6 VPCI 709/P/12 7 VPCI 464/P/1 4 8 VPCI 107/P/14 9 VPCI 672/P/12 10 VPCI 483/P/13 11 VPCI 720/P/14 12 VPCI 1132/P/13 13 VPCI 512/P/14 14 VPCI 249/P/14 15 VPCI 553/P/14 16 VPCI 1047/P/14 17 VPCI 518/P/14 18 VPCI 253/P/14 19 VPCI 540/P/14 20 VPCI 543/P/14 21 VPCI 261/P/1 4 22 VPCI 676/P/12 23 VPCI 480/P/13 24 VPCI 468/P/14 25 VPCI 471/P/13 26 VPCI 677/P/12 27 VPCI 1131/P/13 28 VPCI 708/P/12 29 VPCI 669/P/12 30 VPCI 670/P/12 31 VPCI 475/P/13 32 VPCI 478/P/13 33 VPCI 514/P/1 4 34 VPCI 476/P/13 35 VPCI 507/P/14 36 VPCI 1130/P/13 37 VPCI 245/P/14 38 VPCI 247/P/14 39 VPCI 542/P/14 40 VPCI 250/P/14 41 VPCI 556/P/14 42 VPCI 557/P/14 43 VPCI 1048/P/14 44 VPCI 260/P/14 45 VPCI 550/P/1 4 46 VPCI 509/P/14 47 VPCI 513/P/14 48 VPCI 478/P/14 49 VPCI 671/P/12 50 VPCI 673/P/12 51 VPCI 463/P/14 52 VPCI 266/P/14 53 VPCI 711/P/12 54 VPCI 264/P/14 55 VPCI 265/P/14 56 VPCI 472/P/13 57 VPCI 106/P/14 58 VPCI 263/P/14 59 VPCI 712/P/12 60 VPCI 477/P/13 61 VPCI 479/P/13 62 VPCI 548/P/1 4 63 VPCI 508/P/14 64 VPCI 481/P/13 65 VPCI 484/P/13 66 VPCI 718/P/14 67 VPCI 714/P/14 68 VPCI 248/P/14 69 VPCI 536/P/1 4 70 VPCI 528/P/14 71 VPCI 511/P/14 72 VPCI 510/P/14 73 VPCI 554/P/14 74 VPCI 546/P/14 75 VPCI 1133/P/13 76 VPCI 467/P/14 77 VPCI 473/P/13 78 VPCI 470/P/14 79 VPCI 674/P/12 80 VPCI 270/P/14 81 VPCI 474/P/13 82 VPCI 474/P/14 83 VPCI 459/P/14 84 VPCI 469/P/14 85 VPCI 482/P/13 86 VPCI 1059/P/14 87 VPCI 473/P/14 88 VPCI 692/P/12 89 VPCI 683/P/12 90 VPCI 105/P/14 91 KCTC 17810 92 JCM 15448 93 KCTC 17809
[0109] In some instances, the fungal infection is caused by a fungus in the genus Aspergillus (i.e., an Aspergillus infection). For example, an Aspergillus infection can be caused by a fungus in the genus Aspergillus that is selected from the group consisting of Aspergillus fumigatus, A. flavus, A. terreus, A. niger, A. candidus, A. clavatus, and A. ochraceus. Examples of Aspergillus infections that can be treated by the methods of the invention include, but are not limited to, aspergillosis (e.g., invasive aspergillosis, central nervous system aspergillosis, or pulmonary aspergillosis). In some instances, a fungal infection may also be a dermatophyte infection, which can be caused by a fungus in the genus Microsporum, Epidermophyton, or Trichophyton.
[0110] In some instances, the methods of the invention can be used to treat a Pneumocystis infection, referring to an infection caused by a fungus in the genus Pneumocystis. Fungi in the genus Pneumocystis include P. camii, P. jirovecii, P. murina, P. oryctolagi, and P. wakefieldiae. Examples of Pneumocystis infections that can be treated by the methods of the invention include, but are not limited to Pneumocystis jirovecii pneumonia (also called Pneumocystis camii pneumonia, Pneumocystis pneumonia, or PCP). Further, the methods provided herein can be used to treat, for example, tinea capitis, tinea corporis, tinea pedis, onychomycosis, perionychomycosis, pityriasis versicolor, oral thrush, vaginal candidosis, respiratory tract candidosis, biliary candidosis, eosophageal candidosis, urinary tract candidosis, systemic candidosis, mucocutaneous candidosis, aspergillosis, mucormycosis, paracoccidioidomycosis, North American blastomycosis, histoplasmosis, coccidioidomycosis, sporotrichosis, fungal sinusitis, and chronic sinusitis. Alternatively, the treatment regimens and pharmaceutical compositions described herein can be administered to treat a blood stream infection or organ infection (e.g., lung, kidney, or lover infections) in a subject.
[0111] In some instances, a fungal infection can be a drug-resistant fungal infection, which is a fungal infection that is refractory to treatment with an antifungal drug. In such infections, the fungus that causes the infection is resistant to treatment with one or more antifungal drugs (e.g., an antifungal drug-resistant strain of Candida spp.). Antifungal drugs to which the fungus may be resistant include, but are not limited to, azole compounds, echinocandins, polyene compounds, and flucytosine.
II. Treatment Indications
[0112] The methods of treatment provided herein can be used with (i) a human subject who has one or more indications, symptoms, or signs of a fungal infection or related conditions thereto or (ii) a human subject at high risk of developing a fungal infection or related conditions thereof (e.g., hospital inpatients, intestinal transplant recipients, low birth weight infants, individuals with a genetic susceptibility). The methods disclosed herein may be used alone or in a multi-part treatment plan to treat, mitigate, or prevent conditions, diseases, or symptoms associated with fungal infections or related conditions in a human subject in need or at risk thereof.
[0113] In some instances, an individual who has developed or is at risk of developing a fungal infection can be identified based on standard diagnostic assessments. Such assessments may include testing any appropriate biological sample obtained from the individual in which signs or indicators of the fungal infection are detectable including biological fluid, stool samples, tissue, or cells (e.g., bodily fluids such as blood and blood constituents (e.g., serum and plasma), bronchial lavage sputum, saliva, urine, amniotic fluid, lymph fluid, bile, exudate, peritoneal fluid, cerebrospinal fluid, supernatant from cell lysates, lysed cells, cellular extracts, and nuclear extracts; tissue including tissue from a fresh, frozen and/or preserved organ, tissue sample, biopsy, and/or aspirate). Indicators of infection may be of host origin (e.g., cytokines or antibodies) or microbial origin (e.g., pathogen associated molecules or fungal cells as detected by fecal CFUs, mucosal biopsies, or 16S sequencing).
[0114] Indications of a fungal infection may be directly or indirectly detected in or on the body of the subject. For example, direct signs of an infection include, but are not limited to, detection of overgrowth of an undesired fungal pathobiont or pathogen (e.g., species of Candida) as measured by adherent microbial species on a tissue biopsy or a non-adherent species in other biological sample extractions (e.g., biological fluid, stool samples, tissue, or cells (e.g., bodily fluids such as blood and blood constituents (e.g., serum and plasma), bronchial lavage sputum, saliva, urine, amniotic fluid, lymph fluid, bile, exudate, peritoneal fluid, cerebrospinal fluid, supernatant from cell lysates, lysed cells, cellular extracts, and nuclear extracts; tissue including tissue from a fresh, frozen and/or preserved organ, tissue sample, biopsy, and/or aspirate), wherein the microbe is detected using methods well known in the art (e.g., culture-based methods or non-culture methods). A fungal infection may be indicated by changes (e.g., an increase or decrease) in the abundance of certain fungal taxa, genera (e.g., Candida spp.) or species (e.g., Candida tropicalis, Candida albicans) compared to a healthy individual. Alternatively, a fungal infection may be indicated by a change (e.g., increase or decrease) in the overall abundance or diversity (e.g., composition) of the total population of fungal species compared to a healthy individual.
III. Pharmaceutical Formulations
[0115] The invention features methods for treating or preventing a fungal infection or an associated condition thereto by administering a single dose of a pharmaceutical composition including or consisting of CD101 in salt or neutral form (e.g., by oral, subcutaneous, or intravenous administration). The pharmaceutical composition may be administered to humans with a pharmaceutically acceptable diluent, carrier, and/or excipient. Depending on the mode of administration and the dosage, the pharmaceutical composition of the methods described herein will be formulated into suitable pharmaceutical compositions to permit facile delivery. The single dose may be in a unit dose form as needed. The amount of active component (e.g., CD101 in salt or neutral form) included in the single dose of the invention are such that a suitable dose within the designated range is provided (e.g., a dose of 50 to 800 mg or 500 mg to 1200 mg of CD101 in salt or neutral form).
[0116] A pharmaceutical composition consisting of or including CD101 in salt or neutral form may be formulated for e.g., oral administration, intravenous administration, or subcutaneous administration. In some instances, a pharmaceutical composition consisting of or including CD101 in salt or neutral form may be formulated for oral administration. In some instances, a pharmaceutical composition consisting of or including CD101 in salt or neutral form may be formulated for subcutaneous administration. In some instances, a pharmaceutical composition consisting of or including CD101 in salt or neutral form may be formulated for intravenous administration (e.g., injection or infusion). For injectable formulations, various effective pharmaceutical carriers are known in the art (See, e.g., Remington: The Science and Practice of Pharmacy, 22.sup.nd ed., (2012) and ASHP Handbook on Injectable Drugs, 18.sup.th ed., (2014)).
[0117] Acceptable carriers and excipients in the pharmaceutical composition of the present invention are nontoxic to recipients at the dosages and concentrations employed. Acceptable carriers and excipients may include buffers such as phosphate, citrate, HEPES, and TAE, antioxidants such as ascorbic acid and methionine, preservatives such as hexamethonium chloride, octadecyldimethylbenzyl ammonium chloride, resorcinol, and benzalkonium chloride, proteins such as human serum albumin, gelatin, dextran, and immunoglobulins, hydrophilic polymers such as polyvinylpyrrolidone, amino acids such as glycine, glutamine, histidine, and lysine, and carbohydrates such as glucose, mannose, sucrose, and sorbitol. The compositions may be formulated according to conventional pharmaceutical practice. The concentration of the compound in the formulation will vary depending upon a number of factors, including the dosage of the drug to be administered, and the route of administration.
[0118] Oral Formulations
[0119] The pharmaceutical composition of the present invention (e.g., CD101 in salt or neutral form) can be prepared in the form of an oral formulation. Formulations for oral use can include tablets, caplets, capsules, syrups, or oral liquid dosage forms containing the active ingredient(s) in a mixture with non-toxic pharmaceutically acceptable excipients. These excipients may be, for example, inert diluents or fillers (e.g., sucrose, sorbitol, sugar, mannitol, microcrystalline cellulose, starches including potato starch, calcium carbonate, sodium chloride, lactose, calcium phosphate, calcium sulfate, or sodium phosphate); granulating and disintegrating agents (e.g., cellulose derivatives including microcrystalline cellulose, starches including potato starch, croscarmellose sodium, alginates, or alginic acid); binding agents (e.g., sucrose, glucose, sorbitol, acacia, alginic acid, sodium alginate, gelatin, starch, pregelatinized starch, microcrystalline cellulose, magnesium aluminum silicate, carboxymethylcellulose sodium, methylcellulose, hydroxypropyl methylcellulose, ethylcellulose, polyvinylpyrrolidone, or polyethylene glycol); and lubricating agents, glidants, and antiadhesives (e.g., magnesium stearate, zinc stearate, stearic acid, silicas, hydrogenated vegetable oils, or talc). Other pharmaceutically acceptable excipients can be colorants, flavoring agents, plasticizers, humectants, buffering agents, and the like. Formulations for oral use may also be provided in unit dosage form as chewable tablets, non-chewable tablets, caplets, capsules (e.g., as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium).
[0120] The pharmaceutical compositions of the invention can alternatively be formulated with excipients that improve the oral bioavailability of the compound. For example, the dosage forms of the invention can be formulated for oral administration with medium chain (C8 to C12) fatty acids (or a pharmaceutically acceptable salt thereof), such as capric acid, caprylic acid, lauric acid, or a pharmaceutically acceptable salt thereof, or a mixture thereof. The formulation can optionally include a medium chain (C8 to C12) alkyl alcohol, among other excipients. Alternatively, the compounds of the invention can be formulated for oral administration with one or more medium chain alkyl saccharides (e.g., alkyl (C8 to C14) beta-D-maltosides, alkyl (C8 to C14) beta-D-Gulcosides, octyl beta-D-maltoside, octyl beta-D-maltopyranoside, decyl beta-D-maltoside, tetradecyl beta-D-maltoside, octyl beta-D-glucoside, octyl beta-D-glucopyranoside, decyl beta-D-glucoside, dodecyl beta-D-glucoside, tetradecyl beta-D-glucoside) and/or medium chain sugar esters (e.g., sucrose monocaprate, sucrose monocaprylate, sucrose monolaurate and sucrose monotetradecanoate).
[0121] The methods disclosed herein may also further include the administration of an immediate-release, extended release or delayed-release formulation of CD101 in salt or neutral form.
[0122] Parenteral Formulations
[0123] The pharmaceutical composition of the present invention (e.g., CD101 in salt or neutral form) may be formulated in the form of liquid solutions or suspensions and administered by a parenteral route (e.g., subcutaneous, intravenous, or intramuscular). The pharmaceutical composition can be formulated for injection or infusion. Pharmaceutical compositions for parenteral administration can be formulated using a sterile solution or any pharmaceutically acceptable liquid as a vehicle. Pharmaceutically acceptable vehicles include, but are not limited to, sterile water, physiological saline, or cell culture media (e.g., Dulbecco's Modified Eagle Medium (DMEM), α-Modified Eagles Medium (α-MEM), F-12 medium). Formulation methods are known in the art, see e.g., Gibson (ed.) Pharmaceutical Preformulation and Formulation (2nd ed.) Taylor & Francis Group, CRC Press (2009).
IV. Dosage and Administration
[0124] The methods described herein provide a treatment for a fungal infection by administering a single dose of a pharmaceutical composition including CD101 (e.g., CD101 in salt or neutral form), wherein the single dose is administered in an amount sufficient to treat the fungal infection without requiring additional doses of an antifungal agent. In some instances, the single dose of CD101 (e.g., CD101 in salt or neutral form) is administered without concurrent administration of an additional antifungal agent (e.g., CD101 or another antifungal agent) within a time period (e.g., within 1 min, 30 min, 1 hr, 2 hr, 12 hr, 24 hr, 2 days, 3 days, 4 days, 5 days, 6, days, 1 week before or after administration of the single dose of CD101) that would confer therapeutic benefits (e.g., be systemically active) at the same time that CD101 is at a therapeutically effective concentration in the subject. In some instances, the single dose treatment is not combined with any other antifungal treatment within 1-21 days before or after administration. For example, a single dose of CD101 may be administered (e.g., orally, intravenously, subcutaneously, or intramuscularly) to a subject with a fungal infection and the single dose effectively treats the fungal infection without necessitating additional antifungal treatments before, during, or after the single dose treatment with CD101. In some instances, the individual may have undergone previous but unsuccessful attempts of treatment with a different antifungal agent (e.g., an antifungal agent that does not confer therapeutic benefit) at any time prior to the single dose treatment (e.g., in cases of antifungal-resistant fungal infections) and treatment with a single dose formulation including CD101 (e.g., CD101 in salt or neutral form) is sufficient and effective to treat the infection.
[0125] The dose of CD101 (e.g. CD101 in salt or neutral form) in the present invention depends on factors including the route of administration, the disease to be treated, and physical characteristics, e.g., age, weight, general health, of the human subject). The dose may be adapted by the physician in accordance with conventional factors such as the extent of the disease and different parameters of the subject (e.g., human). Typically, the amount of CD101 (e.g. CD101 in salt or neutral form) contained within one or more doses may be an amount that effectively reduces the risk of or treats a fungal infection and associated conditions in a human subject without inducing significant toxicity.
[0126] The pharmaceutical compositions of the invention can be administered to human subjects in therapeutically effective amounts. The preferred dosage of drug to be administered is likely to depend on such variables as the type and extent of the disorder, the overall health status of the particular human subject, the specific compound being administered, the excipients used to formulate the compound, and its route of administration.
[0127] In some instances, the single dose can include an oral formulation of CD101 (e.g. CD101 in salt or neutral form), and can be administered in doses of about 50 mg to about 1200 mg (e.g., 75±25 mg, 100±25 mg, 150±50 mg, 200±50 mg, 250±50 mg, 300±50 mg, 350±50 mg, 400±50 mg, 500±100 mg, 600±100 mg, 700±100 mg, 1800±100 mg, 1900±50 mg, 1000 mg±500 mg, or 1500±500 mg). In other instances, the single dose of CD101 (e.g. CD101 in salt or neutral form) can include a parenteral formulation (e.g., intravenous, subcutaneous, or intramuscular), and can be administered in dosages of about 50-1200 mg (e.g., 75±25 mg, 100±25 mg, 150±50 mg, 200±50 mg, 250±50 mg, 300±50 mg, 350±50 mg, 400±50 mg, 450±50 mg, 500±100 mg, 600±100 mg, 700±100 mg, 800±100 mg, 900±50 mg, 1000 mg±100 mg, or 1100±100 mg).
[0128] In any of the methods described herein, the timing of the administration of the single dose treatment with CD101 (e.g., CD101 in salt or neutral form) depends on the medical and health status of the human subject. In some instances, the human subject is at risk for developing a fungal infection or a related condition and receives the single dose treatment with CD101 (e.g., CD101 in salt or neutral form) before developing symptoms or signs of a fungal infection. In some instances, the human subject has already developed a fungal infection or a related condition and receives the single dose treatment with CD101 (e.g., CD101 in salt or neutral form). The timing of the administration of the single dose of CD101 (e.g., CD101 in salt or neutral form) may be optimized by a physician to reduce the risk of or to treat a fungal infection in a human subject.
EXAMPLES
Example 1: Subcutaneous Injection of CD101
[0129] Single dose subcutaneous (SC) administration may further extend the utility of CD101 beyond that of other echinocandins, to antifungal treatment and prophylaxis in the outpatient setting. Preclinical studies were conducted to evaluate the feasibility of using SC administration of CD101 for these purposes.
[0130] Methods
[0131] The efficacy of CD101 SC was studied in an immunocompetent DBA/2 mouse model of disseminated candidiasis. Mice (5/grp) were challenged with Candida albicans SC5314 (ATCC: MYA-2876, fluconazole-sensitive human clinical isolate shown to be pathogenic in mice) via IV injection (100 μL, 5.0 log CFU/mouse) and treated with CD101 SC (1, 3 or 10 mg/kg). Micafungin via IP administration was tested as a positive control at the same three doses. At 24 hours following challenge, kidneys were harvested and processed for CFU enumeration. All comparisons were made between the treatment and time-matched vehicle groups. CD101 SC (5 mg/kg) was also tested in a similar disseminated candidiasis model using ICR mice rendered neutropenic by cyclophosphamide on Day −4 (150 mg/kg) and Day −1 (100 mg/kg) prior to infection by the same C. albicans SC5314 strain (IV injection, 100 μL, 4.5 log CFU/mouse, See Example 10).
[0132] Previous toxicology studies by the IV route of administration conducted in cynomolgus monkeys have shown CD101 to be safe and well tolerated at up to at least 30 mg/kg, which generates very high systemic exposures upon initial infusion of CD101 into the bloodstream. Therefore, only local tolerability (and PK) of CD101 by SC administration required evaluation. For this purpose, male and female monkeys were observed for up to 10 days following a single 30 mg/kg SC dose. In the same study, to determine the pharmacokinetics of CD101 following SC administration, whole blood samples were collected and the plasma was harvested at approximately 0.25, 0.5, 1, 2, 4, 8, 24, 36, and 48 hours, and 3, 4, 5, 7, and 10 days postdose. Plasma concentrations were then quantified by liquid chromatography with tandem mass spectrometric detection (LC-MS/MS). Bioavailability from SC dosing was calculated by comparing the calculated area under the concentration-time profile (AUC) from SC against the AUC from IV administration of the same dose.
[0133] Results
[0134] In the DBA/2 mouse efficacy study (
[0135] Early pharmacokinetic studies in rats and monkeys had indicated that CD101 subcutaneous administration was well-tolerated, although these initial studies were aimed at characterizing the pharmacokinetics at lower doses 5 mg/kg). Therefore, a separate study was designed to evaluate the tolerability of a SC dose of CD101 as a highly concentrated solution (100 mg/mL; 30 mg/kg) in two cynomolgus monkeys.
TABLE-US-00002 TABLE 2 Cmax AUClast AUCINF_obs Half- Ani- Dose Tmax (ug/ (hr*μg/ (hr*μg/ life mal Sex (mg/kg) (hr) mL) mL) mL) (hr) 9697 M 30 96 15.9 2740 3280 76.2 9707 F 30 48 10.9 2180 3760 171
TABLE-US-00003 TABLE 3 Component Function Concentration CD101 acetate Active ingredient 100 mg/mL Mannitol Tonicity 11.4 mg/mL HCl pH adjustment As needed to adjust to pH 5.6 NaOH pH adjustment As needed to adjust to pH 5.6 Water for injection medium q.s to 1.0 mL
[0136] In the monkey SC tolerability/PK study, no sign of irritation or local (injection site) adverse toxicity was noted following a single high dose of 30 mg/kg CD101. There was also no effect on bodyweight or food consumption upon further follow-up observations for 10 days after administration.
[0137] From the same monkey SC tolerability/PK study, the pharmacokinetic profile following SC administration of CD101 at 30 mg/kg showed that total exposure measured over a 10-day period was comparable (80% bioavailability) to that following IV administration at the same dose (
TABLE-US-00004 TABLE 4 AUC.sub.last AUC.sub.inf Half- Dose T.sub.max C.sub.max .sub.(μg*hr/ (μg*hr/ life Route (mg/kg) (hr) (μg/mL) mL) mL) (hr) Subcutaneous 30 72 13.4 2460 3520 124 IV 30 1 112 3135 3340 49.7
Example 2: Treatment of a Fungal Infection in a Human Subject with Candidemia by a Single Intravenous Dose of CD101
[0138] A human subject is diagnosed with candidemia using standard diagnostic procedures. The subject receives treatment with a single dose of 50-800 mg (e.g., 75±25 mg, 100±25 mg, 150±50 mg, 200±50 mg, 250±50 mg, 300±50 mg, 350±50 mg, 400±50 mg, 450±50 mg, 500±100 mg, 600±100 mg, 700±100 mg, 800±100 mg, 900±50 mg, 1000 mg±100 mg, or 1100±100 mg) of the acetate salt of CD101 administered by intravenous infusion. No other antifungal treatment is provided to the subject within one to three weeks before or after administration of the single dose CD101 treatment. Following the single intravenous administration of CD101 (e.g., one to three weeks later), the subject is assessed in a follow-up visit and the candidemia infection is confirmed to be resolved.
Example 3: Treatment of a Fungal Infection in a Human Subject with Invasive Candidiasis by a Single Subcutaneous Dose of CD101
[0139] A human subject is diagnosed with invasive candidiasis using standard diagnostic procedures. The subject receives treatment with a single dose of 50-1200 mg (e.g., 75±25 mg, 100±25 mg, 150±50 mg, 200±50 mg, 250±50 mg, 300±50 mg, 350±50 mg, 400±50 mg, 450±50 mg, 500±100 mg, 600±100 mg, 700±100 mg, 800±100 mg, 900±50 mg, 1000 mg±100 mg, or 1100±100 mg) of the acetate salt of CD101 administered by subcutaneous injection. No other antifungal treatment is provided to the subject within one to three weeks before or after administration of the single dose CD101 treatment. Following the single subcutaneous administration of CD101 (e.g., one to three weeks later), the subject is assessed in a follow-up visit and the invasive candidiasis infection is confirmed to be resolved.
Example 4: Treatment of a Fungal Infection in a Human Subject with Aspergillosis by a Single Oral Dose of CD101
[0140] A human subject is diagnosed with aspergillosis using standard diagnostic procedures. The subject receives treatment with a single dose of 50 mg-1200 mg (e.g., 75±25 mg, 100±25 mg, 150±50 mg, 200±50 mg, 250±50 mg, 300±50 mg, 350±50 mg, 400±50 mg, 450±50 mg, 500±100 mg, 600±100 mg, 700±100 mg, 800±100 mg, 900±50 mg, 1000 mg±100 mg, or 1100±100 mg) of the acetate salt of CD101 administered in an oral formulation (e.g., in a pill, capsule, or liquid formulation). No other antifungal treatment is provided to the subject within one to three weeks before or after administration of the single dose CD101 treatment. Following the single oral administration of CD101 (e.g., one to three weeks later), the subject is assessed in a follow-up visit and the aspergillosis infection is confirmed to be resolved.
Example 5: Efficacy of CD101 in Mouse Models of Aspergillosis and Azole-Resistant Disseminated Candidiasis
[0141] Methods
[0142] The in vivo efficacy of CD101 was evaluated using neutropenic mouse models of azole-resistant candidiasis and aspergillosis. An azole-resistant strain of Candida albicans (R357; resistant to fluconazole [Flu], voriconazole, and posaconazole but susceptible to amphotericin B [AmB] and echinocandins) isolated from human blood was used for the mouse candidiasis model. A test strain of Aspergillus fumigatus (ATCC 13073) was used for the mouse aspergillosis model. Mice were rendered neutropenic by cyclophosphamide and then infected by injections of C. albicans (10.sup.5 CFU/mouse) or A. fumigatus (10.sup.4 CFU/mouse) into the tail vein. Test articles were administered starting 2 hours after infection. In the mouse candidiasis model, groups of 5 mice each received one dose of AmB (3 mg/kg IV), Flu (20 mg/kg orally), or CD101 (3, 10 or 30 mg/kg by intraperitoneal administration [IP]). After 72 hours post-infection, mice were euthanized and C. albicans counts in kidney tissue (CFU/g) were measured. In the mouse aspergillosis model, groups of 10 mice each received one dose of AmB (2 mg/kg IP) or CD101 (2 mg/kg IV and IP). Survival was monitored daily for 10 days. Differences between vehicle and test article groups were assessed for significance by one-way ANOVA followed by Dunnett's test and Fisher's Exact test in the candidiasis and aspergillosis models, respectively.
[0143] Results
[0144] One dose of CD101 3 mg/kg produced a >99.9% (or >3-log; P<0.001) reduction in C. albicans CFU compared with vehicle through at least 72 hours post-dose following a single IP dose. AmB showed similar, albeit less robust, efficacy (>99% or >2-log reduction in CFU; P<0.05), whereas fluconazole was less efficacious (83.9% or <2-log reduction in CFU). In the aspergillosis model, CD101 administered 2 mg/kg IV or IP showed similar efficacy to that of AmB 2 mg/kg IP, both with significantly longer survival than vehicle (P<0.05;
Conclusions
[0145] A single dose of CD101 3 mg/kg produced significant reduction in C. albicans burden compared with vehicle (P<0.001) in the neutropenic mouse model of azole-resistant candidiasis, demonstrating efficacy comparable, if not better, to that of AmB at the same dose.
Example 6: Efficacy of CD101 Against Candida auris Clinical Isolates
[0146] Materials and Methods
[0147] Organisms and Antifungal Agents
[0148] C. auris clinical isolates obtained from Japan, South Korea, India and the Center for Medical Mycology (n=14) were evaluated. The following Candida QC strains approved for yeast and moulds by the Clinical and Laboratory Standards Institute (CLSI, Document M38-A2 and M27-A3) were used: C. parapsilosis ATCC 22019, C. krusei ATCC 6258. Test compounds were prepared fresh prior to use in MIC assays and included: CD101, 5-flucytosine (5FC), amphotericin B (AMB), anidulafungin (ANID), caspofungin (CAS), fluconazole (FLU), itraconazole (ITRA), micafungin (MICA), posaconazole (POSA) and voriconazole (VORI).
[0149] Minimum Inhibitory Concentration (MIC) Assays
[0150] Broth microdilution MIC assays performed according to CLSI M38-A2 and M27-A3 methodology were used to evaluate the susceptibility of the fungal strains to the selected antifungals. Briefly, C. auris strains were plated on Sabouraud Dextrose Agar (SDA) and incubated at 37° C. for 2 days. C. auris cells were then harvested then washed in normal saline (0.85% NaCl via centrifugation). MIC assay inoculums were prepared using a hemocytometer. MIC assays were read after 24 and/or 48 hours incubation at 50 and/or 100% inhibition (
Example 7: Efficacy CD101, Caspofungin (CAS), Micafungin (MICA), and Fluconazole (FLU) Against Candida auris Clinical Isolates and FKS1 HS1 Sequence Analysis
[0151] This study was to determine in vitro susceptibility of clinical C. auris isolates to CD101, caspofungin (CAS), micafungin (MICA), and fluconazole (FLU), and to analyze the sequence of hot spot 1 (HS1) within FKS1.
[0152] Materials and Methods
[0153] Candida auris isolates. Thirty-eight C. auris strains, obtained from VP Chest Institute, University of Delhi (Delhi, India) were used in the study (Table 5). Strains were grown on yeast extract peptone dextrose (YPD) agar plates prior to testing.
TABLE-US-00005 TABLE 5 Strain C. auris strain # # (India) 1 VPCI 669/P/12 2 VCPI 671/P/12 3 VCPI 674/P/12 4 VCPI 683/P/12 5 VCPI 692/P/12 6 VCPI 712/P/12 7 VCPI 471/P/13 8 VCPI 475/P/13 9 VCPI 478/P/13 10 VCPI 479/P/13 11 VCPI 480/P/13 12 VCPI 482/P/13 13 VCPI 483/P/13 14 VCPI 1130/P/13 15 VCPI 1132/P/13 16 VCPI 1133/P/13 17 VCPI 105/P/14 18 VCPI 107/P/14 19 VCPI 510/P/14 20 VCPI 511/P/14 21 VCPI 512/P/14 22 VCPI 513/P/14 23 VCPI 514/P/14 24 VCPI 250/P/14 25 VCPI 265/P/14 26 VCPI 266/P/14 27 VCPI 462/P/14 28 VCPI 463/P/14 29 VCPI 467/P/14 30 VCPI 471a/P/14 31 VCPI 478/P/14 32 VCPI 518/P/14 33 VCPI 550/P/14 34 VCPI 714/P/14 35 VCPI 717/P/14 36 VCPI 1060/P/14 37 VCPI 74/P/15 38 VCPI 213/P/15
[0154] Candida auris antifungal susceptibility testing (AFST) Antifungal susceptibility testing was performed in duplicate for each strain in accordance with the guidelines described in CLSI documents M27-A3 (CLSI, 2008). C. parapsilosis ATCC 22019 and C. krusei ATCC 6258 were used as quality control strains. CD101, CAS, MICA, and FLU were obtained as standard powders from their manufacturer, and stock solutions were prepared by dissolving the compounds in water (CAS, MICA) or 100% dimethyl sulfoxide (DMSO) (CD101, FLU).
[0155] FKS1 HS1 PCR/sequencing. FKS1 HS1 PCR was carried out in the T100 thermal cycler (Bio-Rad) in a 30-μl reaction volume using EmeraldAmp MAX PCR Master Mix (TaKaRa). PCR mixtures contained 1 μl of each primer: Cspp_F2275 (5′-AATGGGCTGGTGCTCAACAT-3′) and Cspp_R3070 (5′-CCTTCAATTTCAGATGGAACTTGATG-3′) at 10 μM. A sterile toothpick with a touch of testing single colony was dipped into the PCR reaction mastermix, and then FKS1 HS1 PCR were performed. The time-temperature profile included initial denaturation for 3 min at 94° C. followed by 35 cycles of 30 s at 94° C., 30 s at 53° C., and 90 s at 72° C. Amplicons were visualized on GelStar Nucleic Acid Gel Stain (Lonza) stained 1% agarose gel, purified by using ZR DNA Sequencing Clean-up Kit (Zymo Research), and sequenced by Genewiz. Sequencing results were analyzed by SeqMan Pro 14 (DNASTAR Lasergene).
[0156] Results
[0157] Candida auris antifungal susceptibility testing (AFST). The MIC (μg/ML) distributions of C. auris isolates for CD101, CAS, MICA, and FLU are shown in Table 6. All C. auris isolates (38) were resistant to fluconazole. Four (4) isolates were resistant to all tested echinocandins (CD101, CAS, MICA). CD101 exhibited activity similar to MICA.
[0158] FKS1 HS1 PCR/sequencing. Results of C. auris isolates FKS1 HS1 sequence analysis are shown in Table 6. Thirty four (34) echinocandin-sensitive isolates presented wild-type (WT) genotype within FKS1 HS1 region. Four (4) isolates (strain #s: 16, 25, 27, and 30 in Table 6), demonstrating reduced susceptibility to echinocandins, exhibited serine to phenylalanine amino acid substitution in position equivalent to FKS1 HS1 S645 in Candida albicans.
TABLE-US-00006 TABLE 6 In vitro antifungal susceptibility profile and FKS1 HS1 characteristics of Candida auris strains C. auris Strain strain # CD101 CAS MICA FLU # (India) 24 h 48 h 24 h 48 h 24 h 48 h 24 h 48 h FKS1 HS1 1 VPCI 0.5 0.5 0.25* >16** 0.125 0.25 >128 >128 WT 669/P/12 2 VCPI 0.5 0.5 0.25* >16** 0.125 0.25 >128 >128 WT 671/P/12 3 VCPI 0.25 0.25 0.25* 0.25* 0.06 0.125 >128 128 WT 674/P/12 4 VCPI 0.5 0.5 0.25* >16** 0.125 0.25 >128 >128 WT 683/P/12 5 VCPI 0.5 0.5 0.25* >16** 0.125 0.25 >128 >128 WT 692/P/12 6 VCPI 0.25 0.25 0.25* 0.25* 0.125 0.125 >128 128 WT 712/P/12 7 VCPI 0.5 0.5 1* >16** 0.25 0.25 >128 >128 WT 471/P/13 8 VCPI 0.5 0.5 0.25* 0.25* 0.125 0.25 >128 64 WT 475/P/13 9 VCPI 0.25 0.25 0.25* >16** 0.125 0.125 >128 128 WT 478/P/13 10 VCPI 0.25 0.25 0.5* >16** 0.125 0.125 >128 128 WT 479/P/13 11 VCPI 0.25 0.25 0.5* >16** 0.125 0.125 >128 >128 WT 480/P/13 12 VCPI 0.25 0.25 0.5* >16** 0.125 0.125 >128 >128 WT 482/P/13 13 VCPI 0.25 0.25 0.25* 0.25* 0.125 0.125 >128 128 WT 483/P/13 14 VCPI 0.5 0.25 0.5* 0.5* 0.125 0.125 32 64 WT 1130/P/13 15 VCPI 0.5 0.25 0.5* 0.5* 0.125 0.125 128 128 WT 1132/P/13 16 VCPI 16 >16 16 >16 16 >16 >128 >128 S645F/S 1133/P/13 17 VCPI 0.25 0.25 0.5* 1* 0.125 0.125 128 128 WT 105/P/14 18 VCPI 0.125 0.125 0.25* 0.5* 0.06 0.06 64 >128 WT 107/P/14 19 VCPI 0.25 0.25 0.5* >16** 0.125 0.125 >128 >128 WT 510/P/14 20 VCPI 0.25 0.25 0.5* >16** 0.125 0.125 128 >128 WT 511/P/14 21 VCPI 0.25 0.25 0.5* 1* 0.125 0.125 16 >128 WT 512/P/14 22 VCPI 0.5 0.5 1* >16** 0.125 0.25 >128 >128 WT 513/P/14 23 VCPI 0.5 0.5 0.5* 1* 0.25 0.25 >128 >128 WT 514/P/14 24 VCPI 0.25 0.25 0.5 0.5* 0.125 0.125 64 >128 WT 250/P/14 25 VCPI 16 >16 8 >16 16 >16 >128 >128 S645F 265/P/14 26 VCPI 0.5 0.25 0.125* 0.125* 0.125 0.125 >128 >128 WT 266/P/14 27 VCPI 16 >16 8 >1 16 >16 >128 >128 S645F 462/P/14 28 VCPI 0.125 0.125 0.5* 0.5* 0.125 0.125 >128 >128 WT 463/P/14 29 VCPI 0.25 0.25 0.125* 0.5* 0.25 0.25 >128 >128 WT 467/P/14 30 VCPI 16 >16 4 >16 16 >16 >128 >128 S645F 471a/P/14 31 VCPI 0.5 1 1* 2* 0.5 0.5 >128 >128 WT 478/P/14 32 VCPI 0.5 0.5 0.5* 16** 0.25 0.5 >128 >128 WT 518/P/14 33 VCPI 0.5 1 0.125* 0.25* 0.25 0.5 >128 >128 WT 550/P/14 34 VCPI 0.25 0.25 0.5* >16** 0.125 0.25 >128 >128 WT 714/P/14 35 VCPI 0.25 0.25 0.5* >16** 0.125 0.125 4 >128 WT 717/P/14 36 VCPI 0.25 0.25 0.5* >16** 0.25 0.25 >128 >128 WT 1060/P/14 37 VCPI 0.25 0.25 0.5* >16** 0.25 0.25 >128 >128 WT 74/P/15 38 VCPI 0.25 0.25 0.5* >16** 0.25 0.25 >128 >128 WT 213/P/15 (*CAS paradoxical effect −> 16 μg/ml; **loss of CAS paradoxical effect, no possibility to read MIC, fungal growth reduction <50%)
Conclusions
[0159] High fluconazole resistance is common in clinical isolates of C. auris. Most C. auris strains are susceptible to echinocandins. However, most strains breakthrough on caspofungin at 48 h but not with CD101 or other echinocandins. Highly reduced susceptibility to echinocandins in these C. auris isolates was associated with amino acid substitution (serine into phenylalanine, position equivalent to C. albicans S645) within the FKS1 HS1 region.
Example 8: Efficacy CD101 in the Treatment of Candida auris Infection in a Murine Model of Disseminated Candidiasis
[0160] Methods
[0161] Female 6-8 week old Day −1 mice were immunosuppressed with cyclophosphamide (200 mg/kg) 3 days prior to infection and 150 mg/kg 1 day post-infection. On the day of infection, mice were inoculated with 3×10.sup.7 C. auris blastospores via the lateral tail vein. Mice were randomized into 5 groups (n=5 for colony forming units (CFU) and n=10 for survival): CD101 20 mg/kg administered by intraperitoneal (IP) injection, fluconazole 20 mg/kg administered per os (PO), amphotericin B 0.3 mg/kg IP, and a vehicle control. Treatments were administered 2 hours post-infection (Day 1) and again on Day 4 of the study for a total of 2 doses. Mice were monitored daily and a survival curve was generated. CFU groups were sacrificed on Day 8 of the study. One kidney was removed from each mouse, homogenized, plated on potato dextrose agar (PDA), and incubated at 35° C. for 2 days to determine CFU. The remaining survival mice were monitored until the end of the study (Day 14).
[0162] Results
[0163] CD101 showed an average 3 log reduction in kidney CFU compared to fluconazole, amphotericin B, and vehicle treated groups, which was statistically significant (P=0.03, 0.03, and 0.04, respectively). At the end of the study, percent survival of mice in CD101, fluconazole, amphotericin B, vehicle, and untreated groups was 80, 0, 30, 20, and 0%, respectively (
Conclusion
[0164] Taken together, our findings show that CD101 possesses potent antifungal activity against C. auris infection in a disseminated model of candidiasis. Additionally, treatment with CD101 resulted in a significantly higher overall percent survival.
Example 9: Evaluate the Ability of CD101 to Prevent and Treat Candida albicans Biofilms and Explore its Temporal Effect by Time Lapse Photography
[0165] In this study, we determined the effect of CD101 on prevention and treatment of biofilms formed by Candida albicans in vitro, and evaluated the effect of CD101 (at effective concentration) on formation of biofilm in real time using Time Lapse Microscopy (TLM).
[0166] Materials and Methods
[0167] Test Compounds
[0168] CD101 powder stocks were reconstituted in water or Yeast Nitrogen Base (YNB) medium, and diluted in YNB to a final working concentration of 0.25 μg/ml and 1 μg/ml. YNB with no CD101 was prepared in parallel and used as controls. Fluconazole was used as a comparator.
[0169] Test Media
[0170] YNB and Sabouraud Dextrose Agar (SDA) Media
[0171] CD101 (powder and reconstituted solution) stored at −80° C. when not in use.
[0172] Strains
[0173] C. albicans SC-5314 was used for the current study.
[0174] Activity of CD101 Against Candida Biofilms
[0175] In this study, biofilms were grown in vitro using a biofilm model (Chandra et al., Nature Protocols 3:1909, 2008) and the effect of CD101 on adhesion phase biofilms (representing prevention of biofilms) or mature phase biofilms (representing treatment of biofilms) was determined.
[0176] Activity Against Adhesion Phase (Prevention) or Mature Phase (Treatment) Biofilms
[0177] Biofilms were formed on silicone elastomer (SE) discs using a catheter-associated-biofilm model (Chandra et al., Nature Protocols 3:1909, 2008; Chandra et al., J. Bacteriol. 183: 5385, 2001; Chandra et al., J. Dental Research 80: 903, 2001). For evaluation of activity against adhesion phase biofilms (prevention), Candida cells were adhered to catheter discs for 90 min. Next, discs were incubated for 24 h with CD101 (0.25 or 1 μg/ml concentrations) to allow biofilm formation. For evaluation of activity against mature phase biofilms (treatment), Candida cells were adhered to catheter discs for 90 min, then transferred to fresh media and incubated for a further 24 h to allow formation of biofilms. Mature biofilms were then exposed to CD101 (0.25 or 1 μg/ml concentrations) for another 24 h. Discs incubated with fluconazole or media alone were used as controls in all experiments.
[0178] At the end of drug exposure in both adhesion and mature phase biofilms, biofilms were quantified by measuring their metabolic activity using XTT assay (Chandra et al., Nature Protocols 3:1909, 2008; Chandra et al., J. Bacteriol. 183: 5385, 2001; Chandra et al., J. Dental Research 80: 903, 2001). Following incubation with drugs, discs were transferred to fresh plates containing phosphate buffered saline with XTT and menadione, incubated for 3 hours at 37° C. and optical density was read at 492 nm. Separate batches of biofilms were stained with fluorescent dyes (FUN1™, CONA) and observed under Confocal Scanning Laser Microscope (CSLM) to evaluate biofilm architecture and thickness (Chandra et al., Nature Protocols 3:1909, 2008; Chandra et al., J. Bacteriol. 183: 5385, 2001).
[0179] Time Lapse Microscopy
[0180] The effective CD101 concentration obtained from the above experiments was used to monitor its effect on biofilm formation in real time using TLM, which involves capturing real-time images of a single frame at specific time intervals, allowing temporal monitoring of the interactions occurring between the drug and Candida biofilms. Captured images were combined in a time sequence, resulting in an animation depicting the sequence of events that occurred with the passage of time. Briefly, the discs with C. albicans (adhered for 90 min as above) were placed in a 35-mm-diameter glass-bottom Petri dish (MatTek Corp., Ashland, Mass.). Next, CD101 (dissolved in the growth medium) was added to the Petri dish, and incubated at 37° C. to allow formation of biofilm. Phase contrast images for this interaction were captured immediately from 0 h and followed up to 16-17 hon a Leica DMI 6000 B inverted microscope connected to a Retiga EXi Aqua camera (Q-imaging Vancouver British Columbia). To determine the structural changes in the maturing biofilm, both acquisition and analysis of a series of horizontal (xy) optical sections of the biofilm was done using Metamorph Imaging software (Molecular Devices, Downington, Pa.). Disc incubated with media alone was used as control.
[0181] Statistical Analyses
[0182] Statistical analyses for all data were performed using GraphPad Prism 6 software. Drug treated groups were compared to control untreated groups using unpaired t-tests. P-value of <0.05 was considered significant.
[0183] Results
[0184] Activity Against Adhesion Phase Biofilms (Prevention)
[0185] Our metabolic activity and CSLM results showed that CD101 prevented formation of robust biofilms at both concentrations tested (0.25 and 1 μg/ml). Assessment of metabolic activity revealed that C. albicans treated with CD101 formed significantly less biofilms compared to untreated C. albicans (
[0186] Activity Against Mature Phase Biofilms (Treatment)
[0187] Metabolic activity and CSLM results showed that CD101 was active against mature biofilms at both tested concentrations (0.25 and 1 μg/ml). Mature C. albicans biofilms exposed to CD101 exhibited significantly less metabolic activity compared to those formed by untreated biofilms (
[0188] Time Lapse
[0189] Time lapse movies showed that untreated biofilms formed highly heterogeneous architecture of biofilms with cells/hyphae embedded within extracellular matrix (screen frames in
Conclusion
[0190] Our results demonstrate that CD101 possesses anti-biofilm activity against both adhesion phase and mature phase biofilms formed by C. albicans.
Example 10: Prophylactic, Single-Dose, Subcutaneous Administration of CD101 Shows Robust Efficacy in Neutropenic Mouse Models of Candidiasis and Aspergillosis
[0191] The potential for intermittent subcutaneous (SC) administration of CD101 may extend the utility of CD101 beyond that of other echinocandins, to include antifungal treatment and prophylaxis in the outpatient setting. Neutropenic mouse models of candidiasis and aspergillosis were used to evaluate the in vivo efficacy of single SC doses of CD101 as antifungal prophylaxis.
[0192] Method
[0193] Candidiasis model: ICR mice (5/group) were rendered neutropenic by cyclophosphamide on Day −4 (150 mg/kg) and Day −1 (100 mg/kg), then challenged (Day 0) with Candida albicans ATCC SC5314 via IV (100 μL, 10.sup.5 CFU/mouse). Prior to challenge, mice were given one SC dose (5, 10, or 20 mg/kg) of CD101 on Day −5, Day −3, or Day −1. At 24 hours post-challenge, kidneys were removed for CFU enumeration.
[0194] Aspergillosis model: ICR mice (6/group) were rendered neutropenic by cyclophosphamide on Day −3 (6 mg/mouse), Day +1, and Day +4 (2 mg/mouse). Challenge with Aspergillus fumigatus ATCC via IV (100 μL, 10.sup.4 CFU/mouse) occurred on Day 0. Prior to challenge, mice were given one SC dose (5, 10 or 20 mg/kg) of CD101 on Day −5, Day −3, or Day −1. Survival was monitored for 14 days.
[0195] Results
[0196] In the candidiasis model (
[0197] In the aspergillosis model (
[0198] The pharmacokinetic profile of CD101 in mice following a 10-mg/kg subcutaneous dose shows a half-life of ˜25 hrs with an absolute bioavailability of ˜50% (
Example 11: Efficacy of CD101 in the Treatment of Vulvovaginal Candidiasis in a Rat Model
[0199] Methods and Experimental Design
[0200] Animal Strain. Wistar rats were supplied by Harlan Laboratories UK and were specific pathogen free. Rats weighed 80-100 g at the time of surgery. Ovariectomies were performed. Rats were allowed 4-7 days recovery before transportation to the facility where the experiment was to be performed. Following arrival, rats were allowed at least 4 days acclimatization before start of the experiment. Rats weighed 100-120 g at the time of ovariectomy and were about 300 g at start of the experiment.
[0201] Animal Housing. Rats were housed in sterilized individual ventilated cages that expose the animals at all times to HEPA filtered sterile air. Rats had free access to food and water (sterile) and had sterile aspen chip bedding (changed every 3-4 days). Additionally, during infection, rats had additional access to wet food if required to ensure they remained fully hydrated.
[0202] The room temperature was 22° C.+/−1° C., with a relative humidity of 60% and maximum background noise of 56 dB. Mice were exposed to 12 hour light/dark cycles.
[0203] Pre-conditioning. Female Wistar rats underwent ovariectomy at least 10 days prior to the study commencing. They were further pre-conditioned by treatment with 5 mg/kg 1743-estradiol administered subcutaneously (SC) every other day on Days −7, −5, −3 and −1 prior to infection with C. albicans strain 529. Estradiol treatment continued every other day throughout the study to 7 days post-infection.
[0204] Yeast Isolate. Candida albicans strain 529L was used in this chronic rat vaginal infection model.
[0205] Infection. Yeast strains were inoculated aerobically onto Sabouraud dextrose agar media (SAB) containing 0.05 mg/mL chloramphenicol and incubated at 30° C. for 48-72 h. 18-24 h prior to infection, Yeast Peptone Dextrose (YPD) broths were inoculated with 2-3 isolated colonies from agar plates and incubated overnight (37° C. on an orbital shaker). Broths containing C. albicans strain 529L were washed 3 times with sterile phosphate buffered saline (PBS) before dilution to the correct inoculum for infection. Cell counts were determined using a haemocytometer and confirmed by quantitative culture on Sabouraud dextrose agar.
[0206] Rats were infected with 0.1 mL by intravaginal administration under inhaled isoflurane anaesthesia using about 9.8×10.sup.5 CFU/mL (9.8×10.sup.4 CFU/Rat) C. albicans strain 529L
[0207] Preparation of 17-β-estradiol, CD101, and Fluconazole
[0208] 17-β-estradiol in 20% 2-hydroxpropyl-β-cyclodextrin (HPBCD). 90 mg of 17-β-estradiol (Sigma, UK) was weighed and added to 7.2 g HPBCD (Sigma, UK) and water for infection (WFI) added to obtain a final volume of 36 mL of suspension and used immediately to dose animals at 2.5 mg/mL.
[0209] Vehicle: 12.81 mg/mL Mannitol in WFI. 384.3 mg of mannitol was weighed and 30 mL of WFI was added. The mixture was briefly vortexed until completely solubilized and was filter sterilized using a 0.2 μm filter. This was stored at 2-8° C. until required and was warmed to room temperature before use.
[0210] CD101. To 61.3 mg of CD101 add 12.26 mL of vehicle and mixture briefly vortexed until completely solubilized. This was used neat at 2 mL/kg for the 10 mg/kg dose and was diluted in vehicle 1:2 to prepare the 5 mg/kg dose. These were stored at 2-8° C. until required and were allowed to warm to room temperature before use. Animals were dosed at 2 mL/kg dosing volume by the SC route.
[0211] Fluconazole. Clinical oral suspension was used to prepare fluconazole as follows: 1) Oral suspension was prepared as per manufacturer instructions (10 mg/mL Fluconazole); and 2) The 10 mg/mL oral suspension was further diluted 1:5 in WFI to give 2 mg/mL (20 mg/kg) dosing solution. This was maintained at room temperature until required and animals dosed at 10 mg/mL dosing volume orally (by the PO route).
[0212] Treatment. CD101, fluconazole, and vehicle treatments started at 24 h post infection by the SC route following the dose volume and frequency shown in Table 7. The fluconazole treatment also started at 24 h post infection but was administered by the PO route at the dose volume and frequency shown in Table 7. The study design is further outlined in
TABLE-US-00007 TABLE 7 Treatment End of Dosing Number of commences Total Experiment Group Dose volume Route/ treatment (hours post Number (day post Group No. Treatment (mg/kg) (mL/kg) Regime days infection) of Doses infection) Size 1 Vehicle — 2 SC OD 2 24 2 9 6 2 CD101 5 2 SC OD 1 24 1 9 6 3 CD101 10 2 SC OD 1 24 1 9 6 4 CD101 5 2 SC OD 2 24 2 9 6 5 Fluconazole 20 10 PO OD 1 24 1 9 6 6 Fluconazole 20 10 PO OD 2 24 2 9 6
[0213] Endpoints. The rats were monitored at a frequency appropriate for their clinical condition. Rat weights were recorded at least once daily to ensure animals remained within ethical limits.
[0214] Rats do not typically succumb to infection in this model but untreated rats may experience some weight loss, dehydration, and piloerection. Reduction in weight and general loss of condition due to estradiol treatment are also typical in this rat model. Colonization with C. albicans was determined by quantitative culture of daily vaginal lavage samples. Rats were euthanized 9 days post infection and C. albicans determined by quantitative culture of vaginal tissue (including uterine horns).
[0215] Lavage samples were obtained on Days 1 (pre-treatment), 2, 3, 5, 7, and 9 days post infection by flushing rat vaginas 4 times with 0.1 mL pre-warmed sterile PBS. Following euthanasia, vaginal tissue including uterine horns was removed prior to weighing. Tissues were homogenized in 2 mL sterile PBS using a bead-beater. Vaginal wash and tissue homogenates were diluted appropriately then quantitatively cultured on to Sabouraud dextrose agar containing 0.05 mg/mL chloramphenicol and incubated at 37° C. for up to 72 h before being counted.
[0216] Statistical analysis. Data were analysed using StatsDirect software (version 2.7.8) using the non-parametric Kruskal-Wallis test and if this was statistically significant all pairwise comparisons were analysed (Conover-Inman).
[0217] Results
[0218] In this study, the in vivo efficacy of CD101 dosed SC once at 5 and 10 mg/kg or dosed SC twice at 5 mg/kg was investigated in a rat model of vulvovaginal candidiasis caused by C. albicans strain 529L.
[0219] CD101 and Fluconazole Tolerability and Clinical Condition. CD101 and fluconazole at all treatment dose and duration were well tolerated with no adverse events observed. Animal weights following localized vaginal infection with C. albicans and treatment with CD101 or fluconazole are shown in
[0220] Pharmacokinetic Profile of CD101. The pharmacokinetic (PK) profile of CD101 in female rats (three per group) was characterized. Following subcutaneous (SC) administration, the time to Cmax (i.e. Tmax) was observed between 8 to 24 hours post-dose suggesting slow absorption/distribution from the site of administration (
[0221] Efficacy Data. A robust model of localized C. albicans strain 529L vaginal infection was successfully established. The geometric mean burden of all infected rats was about 0.9×10.sup.3 CFU/mL on Day 1 post infection in pre-treatment vaginal lavage samples (Table 8 and
TABLE-US-00008 TABLE 8 Geometric mean burden on Day 1 post infection in pre-treatment vaginal lavage samples Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/mL) (CFU/mL) (CFU/mL) (CFU/mL) Vehicle SC-Dosed 2.74 × 10.sup.2 6.60 × 10.sup.3 2.44 0.00 Twice CD101 5 mg/kg 9.11 × 10.sup.2 6.11 × 10.sup.3 2.96 −0.52 SC-Dosed Once CD101 10 mg/kg 3.68 × 10.sup.2 1.53 × 10.sup.3 2.57 −0.13 SC-Dosed Once CD101 5 mg/kg 1.83 × 10.sup.3 3.06 × 10.sup.3 3.26 −0.83 SC-Dosed Twice Fluconazole 20 3.16 × 10.sup.3 3.18 × 10.sup.4 3.50 −1.06 mg/kg PO-Dosed Once Fluconazole 20 1.04 × 10.sup.3 2.73 × 10.sup.3 3.02 −0.58 mg/kg PO-Dosed Twice
[0222] The daily lavage data showed the following results: [0223] Day 1 post treatment (Day 2 post infection, Table 9 and
TABLE-US-00009 TABLE 9 Geometric mean burden on Day 1 post treatment (Day 2 post infection) Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/mL) (CFU/mL) (CFU/mL) (CFU/mL) Vehicle SC-Dosed 5.00 × 10.sup.3 3.12 × 10.sup.4 3.70 0.00 Twice CD101 5 mg/kg 3.34 × 10.sup.2 1.92 × 10.sup.3 2.52 1.17 SC-Dosed Once CD101 10 mg/kg 2.48 × 10.sup.2 1.22 × 10.sup.3 2.39 1.30 SC-Dosed Once CD101 5 mg/kg 2.56 × 10.sup.2 2.37 × 10.sup.3 2.41 1.29 SC-Dosed Twice Fluconazole 20 1.50 × 10.sup.2 1.83 × 10.sup.3 2.18 1.52 mg/kg PO-Dosed Once Fluconazole 20 1.27 × 10.sup.2 5.83 × 10.sup.2 2.10 1.59 mg/kg PO-Dosed Twice [0224] Day 2 post treatment (Day 3 post infection, Table 10 and
TABLE-US-00010 TABLE 10 Geometric mean burden on Day 2 post treatment (Day 3 post infection) Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/mL) (CFU/mL) (CFU/mL) (CFU/mL) Vehicle SC-Dosed 3.74 × 10.sup.3 1.21 × 10.sup.4 3.57 0.00 Twice CD101 5 mg/kg 1.21 × 10.sup.2 1.37 × 10.sup.3 2.08 1.49 SC-Dosed Once CD101 10 mg/kg 23.2 1.92 × 10.sup.2 1.37 2.21 SC-Dosed Once CD101 5 mg/kg 1.95 × 10.sup.2 1.07 × 10.sup.4 2.29 1.28 SC-Dosed Twice Fluconazole 20 1.00 0.00 0.00 3.57 mg/kg PO-Dosed Once Fluconazole 20 1.49 4.08 0.17 3.40 mg/kg PO-Dosed Twice [0225] Day 4 post treatment (Day 5 post infection, Table 11 and
TABLE-US-00011 TABLE 11 Geometric mean burden on Day 4 post treatment (Day 5 post infection) Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/mL) (CFU/mL) (CFU/mL) (CFU/mL) Vehicle SC-Dosed 1.65 × 10.sup.4 9.88 × 10.sup.4 4.22 0.00 Twice CD101 5 mg/kg 1.70 × 10.sup.3 9.41 × 10.sup.3 3.23 0.99 SC-Dosed Once CD101 10 mg/kg 1.73 10.6 0.24 3.98 SC-Dosed Once CD101 5 mg/kg 1.73 × 10.sup.3 9.91 × 10.sup.4 3.24 0.98 SC-Dosed Twice Fluconazole 20 1.00 0.00 0.00 4.22 mg/kg PO-Dosed Once Fluconazole 20 1.00 0.00 0.00 4.22 mg/kg PO-Dosed Twice [0226] Day 6 post treatment (Day 7 post infection, Table 12 and
TABLE-US-00012 TABLE 12 Geometric mean burden on Day 6 post treatment (Day 7 post infection) Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/mL) (CFU/mL) (CFU/mL) (CFU/mL) Vehicle SC-Dosed 1.53 × 10.sup.4 1.18 × 10.sup.5 4.18 0.00 Twice CD101 5 mg/kg 4.56 × 10.sup.3 2.39 × 10.sup.4 3.66 0.52 SC-Dosed Once CD101 10 mg/kg 2.59 1.22 × 10.sup.2 0.41 3.77 SC-Dosed Once CD101 5 mg/kg 6.47 × 10.sup.2 1.08 × 10.sup.4 2.81 1.37 SC-Dosed Twice Fluconazole 20 1.00 0.00 0.00 4.18 mg/kg PO-Dosed Once Fluconazole 20 1.00 0.00 0.00 4.18 mg/kg PO-Dosed Twice [0227] Day 8 post treatment (Day 9 post infection, Table 13 and
TABLE-US-00013 TABLE 13 Geometric mean burden on Day 8 post treatment (Day 9 post infection) Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/mL) (CFU/mL) (CFU/mL) (CFU/mL) Vehicle SC-Dosed 1.98 × 10.sup.4 1.38 × 10.sup.5 4.30 0.00 Twice CD101 5 mg/kg 4.58 × 10.sup.3 9.87 × 10.sup.3 3.66 0.64 SC-Dosed Once CD101 10 mg/kg 2.75 1.76 × 10.sup.2 0.44 3.86 SC-Dosed Once CD101 5 mg/kg 1.28 × 10.sup.3 5.28 × 10.sup.3 3.11 1.19 SC-Dosed Twice Fluconazole 20 1.00 0.00 0.00 4.30 mg/kg PO-Dosed Once Fluconazole 20 1.00 0.00 0.00 4.30 mg/kg PO-Dosed Twice
[0228] The lavage burden data are summarized in
[0229] The terminal vaginal tissue burdens (vagina, uterus, and uterine horns) are shown in Table 14 and
TABLE-US-00014 TABLE 14 Terminal vaginal tissue burden (vagina, uterus, and uterine horns) (Day +9 post infection) Group Log Group Log reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/g) (CFU/g) (CFU/g) (CFU/g) Vehicle SC-Dosed 3.11 × 10.sup.5 2.05 × 10.sup.5 5.49 0.00 Twice CD101 5 mg/kg 1.37 × 10.sup.5 4.88 × 10.sup.5 5.14 0.36 SC-Dosed Once CD101 10 mg/kg 5.52 1.16 × 10.sup.4 0.74 4.75 SC-Dosed Once CD101 5 mg/kg 4.00 × 10.sup.4 3.16 × 10.sup.5 4.60 0.89 SC-Dosed Twice Fluconazole 20 1.00 0.00 0.00 5.49 mg/kg PO-Dosed Once Fluconazole 20 1.00 0.00 0.00 5.49 mg/kg PO-Dosed Twice
Summary
[0230] A robust model of localized rat chronic model of vulvovaginal candidiasis following infection with C. albicans strain 529L was established. The infectious burden peaked to >4 Log.sub.10 CFU/mL in lavage samples from the vehicle treatment group. A high level of C. albicans burden was also recovered from vagina, uterus, and uterine horn tissue taken from vehicle control rats.
[0231] Treatment with CD101 administered by the SC route showed the following in lavage wash burdens: [0232] A single dose of 5 mg/kg administered 24 h post infection reduced fungal burden with a peak effect at Day 3 post infection (48 h post treatment) but which was not maintained to the end of the study. Burden reduction was statistically significant vs. vehicle controls only at Day 3 post infection. [0233] A single dose of 5 mg/kg given twice; once at 24 h and another at 48 h post infection resulted in a superior burden reduction compared to the single dose which was maintained for the duration of the study. But like the single dose, statistical significance was only observed at Day 3 post infection. [0234] A single dose at 10 mg/kg (equivalent to 200 mg in human) given at 24 h post infection resulted in substantial reduction in fungal burden at 3 day post infection (48 h post treatment) with a peak effect at 5 day post infection. Thereafter burden appeared to increase again but this was due to a single rat that retained burden whereas all others had actually burdens below the level of detection. These results suggest excellent CD101 distribution/penetration into vaginal mucosa via a single SC dose.
[0235] Treatment with CD101 administered by the SC route showed the following vaginal tissue burden: [0236] A single dose at 5 mg/kg 24 h post infection resulted in a slight reduction in burden. [0237] A single dose at 5 mg/kg given twice; once at 24 h and another at 48 h post infection (total of 2 doses) resulted in a larger decrease in burden compared to the single dose. [0238] A single dose at 10 mg/kg (equivalent to 200 mg in human) given at 24 h post infection resulted in substantial reduction in burden with clearance in fungal burden to below the level of detection in 5 of the 6 rats. Similar to the lavage data, a single rat retained fungal burden. These results suggest excellent CD101 distribution/penetration into vaginal mucosa via a single SC dose.
[0239] All rats treated with fluconazole at 20 mg/kg PO dosed once at 24 h post infection or single dose twice (24 h and 48 h post infection) showed a faster reduction in burden from lavage washes compared to CD101. At the end of the study, all rats had cleared the infection to below the level of detection in both the lavage wash and vaginal tissue.
Example 12: Pharmacodynamics of the Long Acting Echinocandin, CD101, in the Neutropenic Invasive Candidiasis Murine Model Using an Extended Interval Dosing Design
[0240] The current studies included pharmacokinetic/pharmacodynamic (PK/PD) evaluation of CD101 efficacy in a neutropenic murine model of disseminated candidiasis to assist with further clinical development of optimal dosing strategies. The studies were specifically designed to examine [1] pharmacokinetics of extended interval dosing in the murine model; [2] the CD101 dose-response relationships against a diverse group of strains including C. albicans, C. glabrata, and C. parapsilosis; [3] the PK/PD target exposures associated with efficacy against each species. Pharmacokinetic (PK)/pharmacodynamic (PD) targets were examined to provide a framework for further development of clinical dosing regimens, optimize therapy, and assist in establishment of preliminary susceptibility breakpoints.
[0241] Methods
[0242] Antifungal agent. CD101 dose solutions were prepared on the day of experimentation according to manufacturer instructions with 0.9% NaCl, 10% DMSO, and 1% Tween-20.
[0243] Strains. Ten clinical Candida strains were used for the in vivo treatment studies, including four C. albicans, three C. glabrata, and three C. parapsilosis strains (Table 15). This group was selected to encompass phenotypic variability in susceptibility to triazoles and echinocandins and based on similar fitness in the animal model as defined by the amount of growth in control animals over 24 h. The organisms were maintained, grown, and quantified on Sabouraud's dextrose agar (SDA) plates. Select strains used in the study are summarized in Table 15.
TABLE-US-00015 TABLE 15 Study organisms, CD101 susceptibility results, and comparative susceptibility results to anidulafungin. CD101 Anidulafungin MIC MIC Organism Strain (mg/L) (mg/L) C. albicans K-1 0.06 0.015 580 0.06 0.015 98-17 0.06 0.03 98-210 0.03 0.015 C. glabrata 10956 1 1 5592 0.125 0.06 35315 0.5 0.25 C. parapsilosis 20519.069 1 4 20477.048 1 2 20423.072 0.5 1
[0244] In vitro susceptibility testing. All isolates were tested in accordance with the standards in CLSI document M27-A3. The MICs were determined visually after 24 h of incubation as the lowest concentration of drug that causes a significant diminution (≥50%) of growth compared to controls. MICs were determined on three separate occasions in duplicate. Results are expressed as the median of these results.
[0245] Animals. Six-week-old ICR Swiss/CD1 specific-pathogen-free female mice (Harlan Sprague-Dawley, Indianapolis, Ind.) weighing 23 to 27 g were used for all the studies.
[0246] Infection model. A neutropenic, murine, disseminated candidiasis model was used for the treatment studies. The mice were rendered neutropenic (polymorphonuclear cell count, <100/mm3) by injecting 150 mg/kg of cyclophosphamide (Mead Johnson Pharmaceuticals, Evansville, Ind.) subcutaneously 4 days before infection, 100 mg/kg of cyclophosphamide 1 day before infection, and additional cyclophosphamide doses (100 mg/kg) on Day 2 and Day 4 after infection to ensure neutropenia throughout the 168 h (7 d) study period. Three mice were included in each treatment and control group.
[0247] The organisms were subcultured on SDA plates 24 h prior to infection. The inoculum was prepared by placing 3 to 5 colonies into 5 ml of sterile pyrogen-free 0.15 M NaCl warmed to 35° C. The final inoculum was adjusted to a 0.6 transmittance at 530 nm. The fungal count of the inoculum determined by viable counts on SDA was 6.1±0.2 log.sub.10 CFU/ml.
[0248] Disseminated infection with the Candida strains was achieved by injection of 0.1 ml of the inoculum via the lateral tail vein 2 h prior to the start of antifungal therapy. At the end of the study period, the animals were sacrificed by CO2 asphyxiation. The kidneys of each mouse were aseptically removed and placed in 0.15 M NaCl at 4° C. The kidneys were homogenized and serially diluted 1:10, and the aliquots were plated onto SDA for viable fungal colony counts after incubation for 24 h at 35° C. The lower limit of detection was 100 CFU/ml. The results are expressed as the mean CFU/kidney for three mice.
[0249] Pharmacokinetics. Single-dose pharmacokinetic (PK) evaluation was undertaken following intraperitoneal (IP) doses of 1, 4, 16, and 64 mg/kg of CD101. Plasma from groups of three mice per time point (1, 3, 6, 12, 24, 48, and 72-h) was collected. The plasma drug concentrations were determined by liquid chromatography-tandem mass spectrometry. A noncompartmental model was used in the pharmacokinetic analysis. Elimination half-life was calculated by nonlinear least-squares technique. The area under the concentration-time curve (AUC) was calculated by the trapezoidal rule. Pharmacokinetic exposures for doses not directly measured in the PK study were estimated by linear extrapolation for higher and lower dose levels and by interpolation for dose levels within the dose range studied given the linear PK results.
[0250] Treatment efficacy and pharmacodynamic target determination of CD101. Neutropenic mice were infected with one of 10 Candida strains as described above. The dosing regimens were chosen to vary the magnitude of the 24-h AUC/MIC index and to attempt to produce treatment effects that ranged from no effect to a maximal effect. Five dose levels that varied from 0.25 to 64 mg/kg were administered once in a 0.2-ml volume by IP route for the 168 h study period. Due to enhanced effect against single isolate, additional studies at 0.0156 and 0.0625 mg/kg was examined for C. glabrata 5592. Groups of three mice were used for each dosing regimen and control group. At the end of the treatment period (168 h), the mice were euthanized, and their kidneys were immediately processed for CFU determination as described above.
[0251] Data analysis. A sigmoid dose-effect (Hill) model was used to measure the in vivo potency of CD101. The efficacy endpoints included the dose level required to produce a 24 h net static effect (no change in organism burden compared to that at the start of therapy) and the dose required to achieve a 1-log.sub.10 reduction in colony counts (relative to the burden at the start of therapy), when achieved. The maximum response (E.sub.max) was measured as the difference in the number of CFU/kidney relative to that of the untreated control animals. The doses associated with the stasis and 1-log.sub.10 endpoint for each strain was calculated using the equation: log.sub.10 D=[log.sub.10 (E/(E.sub.max−E))/N]+log.sub.10 ED.sub.50, where D is the drug dose, E is the control growth in untreated animals, E.sub.max is the maximal effect, N is the slope of the dose-response relationship, and ED.sub.50 is the dose needed to achieve 50% of the maximal effect. The associated AUC/MIC targets were then calculated for each strain. We used the PK/PD index AUC/MIC in this study as this has been shown to be associated with treatment efficacy in previous in vivo studies with the echinocandins. The calculations were performed using both total and free drug concentrations. The coefficient of determination (R.sup.2) was used to estimate the variance that might be due to regression with the PK/PD index. Kruskal-Wallis one-way analysis of variance (ANOVA) was used to determine if the differences in PK/PD targets were significant between the species.
[0252] Results
[0253] In vitro susceptibility studies. The MICs of CD101 for the selected strains is shown in Table 15. Additionally, given the similarity of CD101 to anidulafungin, the comparative MICs to anidulafungin are shown. Of note, the strains included those with known resistance (C. glabrata 10956 is echinocandin resistant secondary to FKS mutation FKS2_HS1_F659V) or reduced susceptibility (C. glabrata 35315) to echinocandins. Overall, the CD101 MIC varied by 32-fold for all strains.
[0254] Pharmacokinetics. The time course of plasma concentrations of CD101 in mice after intraperitoneal doses of 1, 4, 16, and 64 mg/kg are shown in
[0255] Treatment efficacy and pharmacodynamic target determination of CD101. At the start of therapy, mice had 4.2±0.2 log.sub.10 CFU/kidney and burden increased in untreated controls to 7.2±0.6 log.sub.10 CFU/kidney. The in vivo dose-response curves for each group of organisms is shown in
[0256] The doses necessary to achieve net stasis and 1-log.sub.10 kill (when endpoint was achieved) are shown in Table 16. The corresponding total and free drug AUC/MIC values for the stasis and
[0257] 1-log.sub.10 kill endpoints are shown for the total experiment duration of 168 h (7 d). As above, also shown in the table is the average 24 h free drug AUC/MIC targets to allow for comparison to other echinocandin studies in this model. Stasis was achieved against all but a single strain and 1-log.sub.10 kill was achieved against all C. albicans and C. glabrata but none of the C. parapsilosis strains. The median stasis free drug AUC.sub.0-168/MIC targets for each organism group was: C. albicans 20.5, C. glabrata 0.5, and C. parapsilosis 18.2 (only two strains achieved the endpoint). The median stasis 24 h free drug AUC/MIC targets were: C. albicans 2.92, C. glabrata 0.07, and C. parapsilosis 2.61. The PK/PD targets for 1-log.sub.10 kill endpoint were 2-4 fold higher than stasis targets indicating a relatively steep exposure-response relationship.
TABLE-US-00016 TABLE 16 Static and 1-log kill doses and associated AUC/MIC values in the neutropenic disseminated candidiasis model. Stasis Stasis Stasis 1 log kill 1 log kill 1 log kill Static total drug free drug 24 h Ave 1 log kill total drug free drug 24 h Ave MIC dose AUC.sub.0-168 h/ AUC.sub.0-168 h/ free drug dose AUC.sub.0-168 h/ AUC.sub.0-168 h/ Free drug Organism Strain (mg/L) (mg/kg) MIC MIC AUC/MIC (mg/kg) MIC MIC AUC/MIC C. albicans K-1 0.06 2.52 3197.16 25.58 3.65 5.26 6005.95 48.05 6.86 580 0.06 1.20 1769.30 14.15 2.02 2.03 2667.21 21.34 3.05 98-17 0.06 1.34 1918.43 15.35 2.19 2.73 3433.40 27.47 3.92 98-210 0.03 1.06 3241.65 25.93 3.70 2.28 5875.95 47.01 6.72 Mean 1.53 2531.64 20.25 2.89 3.08 4495.63 35.97 5.14 Median 1.27 2557.79 20.46 2.92 2.51 4654.68 37.24 5.32 St Dev 0.67 796.71 6.37 0.91 1.49 1698.80 13.59 1.94 C. glabrata 10956 1 6.29 418.68 3.35 0.48 17.25 1052.22 8.42 1.20 5592 0.125 0.06 43.16 0.35 0.05 0.43 317.50 2.54 0.36 35315 0.5 0.34 62.50 0.50 0.07 2.39 367.06 2.94 0.42 Mean 2.23 174.78 1.40 0.20 6.69 578.93 4.63 0.66 Median 0.34 62.50 0.50 0.07 2.39 367.06 2.94 0.42 St Dev 3.52 211.44 1.69 0.24 9.20 410.63 3.29 0.47 C. 20519.069 1 NA* NA parapsilosis 20477.048 1 52.96 3339.42 26.72 3.82 NA 20423.072 0.5 9.62 1217.49 9.74 1.39 NA *NA, not achieved
Discussion
[0258] In the current murine model pharmacodynamic study, we aimed to integrate the pharmacokinetic properties and in vitro potency to provide guidance on pharmacodynamic targets associated with efficacy against a clinically relevant and diverse group Candida spp. Indeed, the pharmacokinetics of CD101 were unique in that the elimination half-life in mice was prolonged (range 29-41 h). For comparison purposes, the half-life of other echinocandins in the same murine model are on average approximately 14 h. We also demonstrated promising in vitro potency against Candida spp. similar to previous larger surveillance antimicrobial susceptibility studies. Finally, we demonstrated CD101 has favorable in vivo efficacy using the murine disseminated candidiasis model with numerically lower PK/PD target exposures for most organisms compared to other echinocandins. For example, the median stasis 24 h free drug AUC/MIC against C. albicans was 2.92. This is 5- to 10-fold lower than caspofungin, micafungin, and anidulafungin targets against this species. An even larger difference was demonstrated for C. glabrata where CD101 free AUC/MIC targets were >10-fold lower than the three comparator echinocandins. C. parapsilosis PK/PD target analysis was limited in the current study as only two strains were evaluable for the stasis target endpoint, but here too CD101 free AUC/MIC targets were numerically lower than the three comparator echinocandins. It is important to note that due to the prolonged half-life, mice were protected from organism growth and disease for a neutropenic duration of 7 days. Taken together, the study demonstrates that CD101 is a potential valuable addition to the antifungal armamentarium given its unique pharmacokinetic properties and in vivo efficacy.
[0259] An important consideration in translating pre-clinical PK/PD target models to clinical medicine is to examine the targets identified in the context of human pharmacokinetics and surveillance susceptibility ranges. Pharmacokinetic study of CD101 in humans demonstrated a free drug AUC.sub.0-168 of 30.2 mg*h/L for a 400 mg dose and 15.4 mg*h/L for a 200 mg dose. This would translate into an average 24 h AUC of approximately 4.3 and 2.2 mg*h/L, respectively, over a 7 day period. Thus, if a patient were to receive 400 mg of CD101 on Day 1 followed by a 200 mg on Day 8 to complete two weeks of therapy, the stasis target would be expected to be achieved against all C. albicans and C. parapsilosis isolates with MIC 1 mg/L, and against all C. glabrata with MIC 16 mg/L. The potency against C. glabrata, including an FKS mutant strain included in this study, deserves particular attention to further study given the rise of echinocandin resistance within this species. Overall, the data suggests CD101 exposures in humans would be expected to meet or exceed the stasis targets identified in this study for nearly all wild-type isolates for the examined species.
[0260] In summary, CD101 is a promising, novel echinocandin in development with advantageous pharmacokinetic properties allowing for once weekly dosing strategies, which would mitigate risks to patients as well as conservation of health care resources and potentially lower expenditures. CD101 has demonstrable in vitro and in vivo potency that is either equivalent or improved upon comparator echinocandins, especially in regards to C. glabrata. Single doses provided 7 days of potent antifungal activity in a well-established immunocompromised disseminated candidiasis model. Importantly, the PK/PD targets identified suggest that current studies of intermittent dosing strategies (i.e. once weekly infusions) of CD101 are likely to be efficacious in humans against the majority of C. albicans, C. glabrata, C. parapsilosis strains. The studies indicate continued clinical evaluation and development for the treatment and prevention of invasive candidiasis as well as other potential fungal infections should be pursued.
Example 13: Efficacy of CD101 in a Murine Model of Pulmonary Aspergillosis
[0261] This study assessed the antifungal efficacy of CD101 by intraperitoneal administration in a murine model of pulmonary aspergillosis caused by Aspergillus fumigatus (strain AF293) compared to micafungin. The primary objective of the study was to compare survival between the treatment groups.
[0262] Methods
[0263] Animal Strain and housing. Mice used in these studies were supplied by Charles River (Margate UK) and were specific pathogen free. The strain of mice used was ICR (also known as CD1 Mice) which is a well characterized outbred murine strain. Mice (male) were 11-15 g on receipt at our facility and were allowed to acclimatize for at least seven days.
[0264] Immunosuppression. Mice were immunosuppressed on Day −4 with 150 mg/kg cyclophosphamide IP, and on Day −1 with 150 mg/kg cyclophosphamide IP and 175 mg/kg cortisone acetate SC. To prevent bacterial infection due to the immunosuppression mice were given 50 mg/kg/day ceftazidime.
[0265] Preparation of Organism and Infection. A. fumigatus strain AF293 inoculum was prepared from spore cultures grown on Sabouraud Dextrose agar (SAB) containing 50 μg/mL chloramphenicol (SABC) in vented tissue culture flasks. Following incubation for 7-10 days at 30° C., spore cultures were washed in sterile phosphate buffered saline (PBS) containing 0.05% Tween 80. Spore count was determined using a haemocytometer and spores were diluted in PBS to ˜6.9×10.sup.6 CFU/mL. Inoculum concentration was confirmed by quantitative culture onto SABC agar. Neutropenic mice lungs were infected with 0.04 mL (0.02 mL/nares) of ˜6.9×10.sup.6 CFU/mL (˜2.8×10.sup.5 cfu/mouse) of A. fumigatus strain AF293 by intranasal (IN) instillation under temporary 2.5% isoflurane induced anesthesia.
[0266] Preparation of Test Articles. Micafungin was provided as a 50 mg vial (Lot 02323002, expiry August 2017) and was prepared as per manufacturer instructions by adding 5 mL saline for injection (SFI) directly into the vial to make a 10 mg/mL stock solution. This solution was then diluted further in SFI to a working concentration of 0.2 mg/mL. The compound was administered IP at 10 mL/kg to achieve a 2 mg/kg dose. It was prepared fresh once and stored at 4° C. between doses.
[0267] Vehicle and CD101 diluent was 10% DMSO/1% Tween 20 in SFI: 1 mL of Tween 20 was added to 10 mL DMSO and the gently mixed and SFI added to a final volume of 100 mL. This was filter sterilised and maintained at room temperature before use for dosing or formulating CD101. The vehicle was administered IP at 10 mL/kg.
[0268] Test article CD101 stock was prepared at 2 mg/mL in 10% DMSO/1% Tween 20 diluent. A clear non particulate solution was obtained following gentle mixing. The stock was kept at 4° C. until required. Study doses of 5 mg/kg (0.5 mg/mL) and 10 mg/kg (1 mg/mL) were prepared from the 2 mg/mL stock as required by diluting in 10% DMSO/1% Tween 20 diluent. The 2 mg/mL stock was used undiluted for the 20 mg/kg study dose. All doses were administered IP at 10 mL/kg.
[0269] Treatment. For this study, treatments were initiated on day five pre-infection according to treatment groups outlined in Table 17. A total of 78 mice (six mice per treatment group) were used in the study.
TABLE-US-00017 TABLE 17 Murine model of pulmonary aspergillosis treatment groups Test Dosing Conc. mg/mL Total Mice End of Group Article Route Schedule Day ml/kg mg/kg Dosage Dose (ICR) study 1 Vehicle IP Single −5 — — — — 6 10 2 Micafungin IP Single 0* 0.2 10 2 2 6 10 3 Micafungin IP Single −1 0.2 10 2 2 6 10 4 CD101 IP Single 0* 0.5 10 5 5 6 10 5 CD101 IP Single −1 0.5 10 5 5 6 10 6 CD101 IP Single −3 0.5 10 5 5 6 10 7 CD101 IP Single −5 0.5 10 5 5 6 10 8 CD101 IP Single −1 1 10 10 10 6 10 9 CD101 IP Single −3 1 10 10 10 6 10 10 CD101 IP Single −5 1 10 10 10 6 10 11 CD101 IP Single −1 2 10 20 20 6 10 12 CD101 IP Single −3 2 10 20 20 6 10 13 CD101 IP Single −5 2 10 20 20 6 10 *1 h post infection
[0270] General Health monitoring. The mice were monitored at a frequency appropriate for their clinical condition. Mouse weights were recorded at least once daily both to ensure animals remained within ethical limits and to monitor efficacy of treatment.
[0271] Endpoints. The primary endpoint for this study was survival within agreed ethical limits (>20% weight loss, severe hypothermia <34° C., inability to reach food or drink, severe hunching). Mice were monitored by daily weight measurements with observations as frequently as clinical condition required. Mice presenting with severe clinical deterioration were humanely euthanized using an overdose of pentobarbitone administered by IP injection following clinical assessment and the time of death was recorded. Animal carcasses were stored at −20° C. for assessment of burden. Ten days post infection all surviving animals were weighed and had their clinical condition assessed prior to being euthanized. Final survival numbers were recorded and analyzed as described below and carcasses frozen at −20° C. prior to further processing.
[0272] A secondary endpoint for the study was terminal lung tissue burden. Immediately following confirmation of death, carcasses were frozen at −20° C. prior to tissue dissection and processing. The frozen carcasses were thawed at room temperature and the lungs removed and placed into pre-weighed bead-beating tubes containing 2 mL of PBS and subjected to mechanical disruption. Organ homogenates were diluted further in PBS and quantitatively cultured for A. fumigatus onto SABC and incubated at 30° C. for 24-48 hours. In addition, a 300 μL aliquot of the undiluted lung tissue homogenate was stored at −80° C. for possible optional assessment of burden by qPCR.
[0273] Statistical analysis. Data were analyzed using StatsDirect software (version 2.7.8). Survival data were analyzed using the Kaplan Meier and Log-Rank and Wilcoxon tests (using the Peto-Prentice weighting method).
[0274] Results
[0275] The aim of this study was to determine the in vivo efficacy of CD101 in a murine model of pulmonary aspergillosis. The design of this study is summarized in Table 17. All treatments were well tolerated with no adverse signs observed.
[0276] Body weights. Animal weights following infection with A. fumigatus strain AF293 are shown in
[0277] Survival. The median and mean survival for the various treatments are shown in Table 18 and the survival plots for all treatment groups are shown in
TABLE-US-00018 TABLE 18 Mean and median survival per treatment group Median Mean Survival Survival Treatment (Hours) (Hours) Vehicle IP Day −5 52.5 69.0 Micafungin 2 mg/kg IP Day 0 73.3 75.3 Micafungin 2 mg/kg IP Day −1 64.7 64.7 CD101 5 mg/kg IP Day 0 64.6 67.8 CD101 5 mg/kg IP Day −1 67.6 72.1 CD101 5 mg/kg IP Day −3 67.7 70.0 CD101 5 mg/kg IP Day −5 65.3 65.3 CD101 10 mg/kg IP Day −1 81.0 121.8 CD101 10 mg/kg IP Day −3 73.4 76.9 CD101 10 mg/kg IP Day −5 65.7 67.2 CD101 20 mg/kg IP Day −1 72.3 155.6 CD101 20 mg/kg IP Day −3 69.8 91.9 CD101 20 mg/kg IP Day −5 69.8 75.5
[0278] A robust survival model of pulmonary aspergillosis infection with A. fumigatus strain AF293 was established. Vehicle treated mice started to succumb to the infection ˜48 h post infection and all had succumbed to the infection by Day 5 post infection resulting in a mean survival time of 69 h post infection. The study was terminated 10 days post infection as most mice had succumbed to the infection.
[0279] Survival in animal groups treated with CD101 was compared against groups treated with the comparator micafungin at the same time pre- or post-infection. Groups treated with 10 mg/kg and 20 mg/kg CD101 one day before infection had statistically greater survival compared to groups treated with micafungin one day before infection (Table 19).
TABLE-US-00019 TABLE 19 Log-rank and Wilcoxon test output for different comparisons Comparison Log-Rank Peto-Prentice Vehicle vs. Micafungin 2 mpk Day 0 NS NS Vehicle vs. Micafungin 2 mpk Day −1 NS NS Vehicle vs. CD101 5 mpk Day 0 NS NS Vehicle vs. CD101 5 mpk Day −1 NS NS Vehicle vs. CD101 5 mpk Day −3 NS NS Vehicle vs. CD101 5 mpk Day −5 NS NS Vehicle vs. CD101 10 mpk Day −1 NS NS Vehicle vs. CD101 10 mpk Day −3 NS NS Vehicle vs. CD101 10 mpk Day −5 NS NS Vehicle vs. CD101 20 mpk Day −1 NS (0.0533) 0.0465 Vehicle vs. CD101 20 mpk Day −3 NS NS Vehicle vs. CD101 20 mpk Day −5 NS NS Micafungin 2 mpk Day 0 vs. CD101 5 mpk Day 0 NS NS Micafungin 2 mpk Day −1 vs. CD101 5 mpk Day −1 NS 0.0467 Micafungin 2 mpk Day −1 vs. CD101 10 mpk Day −1 0.0201 0.0191 Micafungin 2 mpk Day −1 vs. CD101 20 mpk Day −1 0.0047 0.0067 CD101 5 mpk Day −1 vs. CD101 10 mpk Day −1 NS NS CD101 5 mpk Day −1 vs. CD101 20 mpk Day −1 NS NS CD101 5 mpk Day −3 vs. CD101 10 mpk Day −3 NS NS CD101 5 mpk Day −3 vs. CD101 20 mpk Day −3 NS NS CD101 5 mpk Day −5 vs. CD101 10 mpk Day −5 0.0009 0.0015 CD101 5 mpk Day −5 vs. CD101 20 mpk Day −5 0.0009 0.0015 CD101 5 mpk Day 0 vs. CD101 5 mpk Day −1 NS NS CD101 5 mpk Day 0 vs. CD101 5 mpk Day −3 NS NS CD101 5 mpk Day 0 vs. CD101 5 mpk Day −5 NS NS CD101 5 mpk Day −1 vs. CD101 5 mpk Day −3 NS NS CD101 5 mpk Day −1 vs. CD101 5 mpk Day −5 NS NS CD101 5 mpk Day −3 vs. CD101 5 mpk Day −5 0.0183 0.0426 CD101 10 mpk Day −1 vs. CD101 10 mpk Day −3 NS NS CD101 10 mpk Day −1 vs. CD101 10 mpk Day −5 NS NS CD101 10 mpk Day −3 vs. CD101 10 mpk Day −5 NS NS CD101 20 mpk Day −1 vs. CD101 20 mpk Day −3 0.0387 0.033 CD101 20 mpk Day −1 vs. CD101 20 mpk Day −5 NS NS CD101 20 mpk Day −3 vs. CD101 20 mpk Day −5 NS NS NS-not significant
[0280] Lung burden. Terminal lung burden are shown in Table 20 and
TABLE-US-00020 TABLE 20 Lung burden Group Log.sub.10 Group Log.sub.10 reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/g) (CFU/g) (CFU/g) (CFU/g) Vehicle IP Day −5 5.93 × 10.sup.3 5.67 × 10.sup.4 3.77 0.00 Micafungin 2 mg/kg IP Day 0 1.08 × 10.sup.4 3.10 × 10.sup.4 4.03 −0.26 Micafungin 2 mg/kg IP Day −1 4.34 × 10.sup.4 2.65 × 10.sup.4 4.64 −0.86 CD101 5 mg/kg IP Day 0 5.65 × 10.sup.4 1.28 × 10.sup.5 4.75 −0.98 CD101 5 mg/kg IP Day −1 3.75 × 10.sup.4 3.75 × 10.sup.4 4.57 −0.80 CD101 5 mg/kg IP Day −3 5.71 × 10.sup.4 5.21 × 10.sup.4 4.76 −0.98 CD101 5 mg/kg IP Day −5 6.36 × 10.sup.4 2.99 × 10.sup.4 4.80 −1.03 CD101 10 mg/kg IP Day −1 5.17 × 10.sup.3 5.89 × 10.sup.4 3.71 0.06 CD101 10 mg/kg IP Day −3 7.34 × 10.sup.3 3.39 × 10.sup.4 3.87 −0.09 CD101 10 mg/kg IP Day −5 3.40 × 10.sup.4 1.97 × 10.sup.4 4.53 −0.76 CD101 20 mg/kg IP Day −1 1.12 × 10.sup.4 3.46 × 10.sup.4 4.05 −0.28 CD101 20 mg/kg IP Day −3 4.92 × 10.sup.4 4.12 × 10.sup.4 4.69 −0.92 CD101 20 mg/kg IP Day −5 8.35 × 10.sup.3 3.58 × 10.sup.4 3.92 −0.15
Conclusions
[0281] In this model of pulmonary aspergillosis, mice developed robust infection with ˜80% vehicle treated mice succumbing to the infection by Day 4 post infection and 100% mice by Day 5 post infection.
[0282] Single dose CD101 treatment one day pre-infection at 10 mg/kg or 20 mg/kg (the CD101 human dose (400 mg) AUC equivalent) resulted in statistically greater survival compared to comparator 2 mg/kg (the micafungin human dose (50 mg) AUC equivalent) micafungin treatment one day pre-infection.
Example 14: CD101 Prophylactic Dose Rationale for Prevention of Aspergillus, Candida, and Pneumocystis Infections
[0283] Clinical pharmacokinetics of CD101 were compared to measures of nonclinical in vitro susceptibility and in vivo efficacy to guide dose selection for prevention of fungal infections.
[0284] Methods
[0285] The protein binding of CD101 to mouse and human plasma proteins was measured by ultracentrifugation, where free compound is separated from protein-bound compound after 2.5 hr at 37° C. by sedimentation using high centrifugal force. Concentrations in plasma ranging from 7 to 60 μg/mL were tested and resulting samples were analyzed by LC-MS/MS.
[0286] The in vitro activity of CD101 was previously evaluated as part of the SENTRY international surveillance program using CLSI broth microdilution methodology (M38-A2, M27-A3; Pfaller, et al 2017). CD101 demonstrated potent activity against Aspergillus fumigatus (MEC.sub.90=0.015 μg/mL) and Candida albicans (MIC.sub.90=0.06 μg/mL) clinical isolates. These susceptibility data were then compared graphically to CD101 plasma concentrations from studies in healthy adults, adjusted for plasma protein binding. Nonclinical efficacy in a murine model of Pneumocystis pneumonia were also considered to evaluate CD101 doses for clinical investigation of antifungal prophylaxis.
[0287] Results
[0288] In the protein binding study, across the concentrations tested, the percent of bound CD101 ranged from 96.4% to 98.0% with a mean of 97.4% in human plasma, whereas the percent of bound CD101 ranged from 99.2% to 99.3% with a mean of 99.2% in mouse plasma.
[0289] Mean unbound CD101 plasma concentrations in Phase 1 subjects following a single dose of 400 mg were above the MIC.sub.90 for C. albicans for seven days, and CD101 plasma concentrations for both 400 mg and 200 mg were above the MEC.sub.90 for A. fumigatus for 7 days (
Example 15: In Vitro Activity and In Vivo Tissue Distribution of CD101
[0290] The in vitro activity of CD101 was evaluated against 153 A. fumigatus clinical isolates collected as part of the 2014 and 2015 JMI international SENTRY surveillance program. Susceptibility was determined by measuring the minimal effective concentration (MEC) values in accordance with CLSI broth microdilution guidelines (M38-A2). In vivo tissue distribution of CD101 in SD rats (N=3/time up to 5 d) after a 5 mg/kg IV CD101 dose. Plasma/tissue concentrations were measured by LC-MS/MS.
[0291] CD101 demonstrated potent in vitro activity against clinical A. fumigatus isolates with MEC50, MEC90 and MEC range values of 0.015, 0.015, and 0.0078-0.03 μg/mL, respectively.
[0292] In vivo, CD101 tissue/plasma exposure ratios (˜4) were comparable among the major organs (liver, kidney, lung, spleen) suggesting efficient penetration. Also, longer tissue residence times were observed as t.sub.1/2 of CD101 in all tissues (40-77 h) studied were longer compared with plasma (39 h) (
Example 16: A. fumigatus (ATCC 13073) Disseminated Infection of Neutropenic ICR Mice: CD101 Prophylactic Efficacy
[0293] The study objective was to evaluate the efficacy of the test article, CD101, as prophylaxis in the Aspergillus fumigatus (ATCC 13073) disseminated infection model with neutropenic ICR mice.
[0294] Methods
[0295] Inoculum Preparation. A. fumigatus (ATCC 13073) growth was taken from 96 h potato dextrose agar (PDA) and re-suspended in 0.1% Tween 20. The culture was resuspended in 1 mL cold PBS (>1.0×10.sup.8 CFU/mL, OD620 2.3-2.8). The culture was then diluted in PBS to final cellular densities of 2.0×10.sup.5 CFU/mL. The actual colony counts were determined by plating dilutions on PDA plates to confirm inoculation concentration. The actual inoculum count was 1.85×10.sup.5 CFU/mL.
[0296] A. fumigatus (ATCC 13073) disseminated infection (IV). Groups of 6 female ICR mice weighing 22±2 g were used. Animals were immunosuppressed by three intraperitoneal (IP) injections of cyclophosphamide (the first at 6 mg/mouse 3 days before inoculation, the second and third at 2 mg/mouse on Day 1 then Day 4 after inoculation). On Day 0, animals were inoculated (0.1 mL/mouse) by intravenous (IV) injection into the tail vein with A. fumigatus (ATCC 13073), 1.85×10.sup.4 CFU per mouse. CD101 at 5, 10 and 20 mg/kg as prophylaxis was administered subcutaneously (SC) once starting 5, 3 or 1 day before inoculation. In addition, CD101 at 3 mg/kg SC and the reference, amphotericin B, at 3 mg/kg by intraperitoneal (IP) injection were administered one hour after infection (See Table 21).
[0297] Mortality was observed for 14 days. A 50 percent or more 50%) increase in the survival rate compared to the vehicle control group indicates significant anti-infective activity. The health observations including body weight, hunched posture, ruffled fur, immobility and hypothermia were recorded daily for 14 days. Animals found moribund were to be humanely sacrificed with CO2 asphyxiation in the study.
TABLE-US-00021 TABLE 21 Study design Group Article Route Schedule Day mg/mL mL/kg mg/kg Dose (ICR) 1 Vehicle — None — — — — — 6 2 AmpB IP Single .sup. 0.sup.a 0.3 10 3 3 6 3 CD101 SC Single .sup. 0.sup.a 0.5 10 5 5 6 4 CD101 SC Single −5 0.5 10 5 5 6 5 CD101 SC Single −3 0.5 10 5 5 6 6 CD101 SC Single −1 0.5 10 5 5 6 7 CD101 SC Single −5 1 10 10 10 6 8 CD101 SC Single −3 1 10 10 10 6 9 CD101 SC Single −1 1 10 10 10 6 10 CD101 SC Single −5 2 10 20 20 6 11 CD101 SC Single −3 2 10 20 20 6 12 CD101 SC Single −1 2 10 20 20 6
[0298] Results
[0299] Subcutaneous administrations of CD101 at 5, 10, and 20 mg/kg on Day −5, −3 and −1 were associated with significant 50%) increase in the 14-day survival compared to the vehicle group (
[0300] In addition, the symptoms of infection including a decrease in the body weight, hunched posture, ruffled fur, immobility and hypothermia from were improved by subcutaneous administrations of CD101 at 5, 10 and 20 mg/kg on Day −5, −3 and −1 before infection.
Example 17: CD101 Tissue and Epithelial Lining Fluid Concentrations Substantiates its Use for Prophylaxis Treatment as Evident in Mouse Disseminated and Pulmonary Apergillosis
[0301] CD101 has previously demonstrated robust efficacy in mouse antifungal models of aspergillosis. The distribution of CD101 into lung epithelial lining fluid (ELF) was studied to provide further substantiation of observed efficacy.
[0302] Methods
[0303] CD101 (20 mg/kg) was administered by IP to 24 ICR mice. At pre-dose, 1, 3, 6, 12, 24, 48, and 72 hours post-dose, 3 mice/timepoint were anesthetized/euthanized for blood collection (plasma) and bronchoalveolar lavage fluid (BALF) collection with 2×0.5 mL flushes of saline. Urea levels for plasma/BALF normalization for the volume of lung epithelial lining fluid (ELF) calculation were quantified using a commercially-available spectrophotometry-based assay. CD101 concentrations in plasma/BALF samples were measured by LC with electrospray ionization tandem mass spectrometric (LC-MS/MS) detection.
[0304] Disseminated aspergillosis: ICR mice (6/grp) were made neutropenic by cyclophosphamide on Days −3 (270 mg/kg), +1 and +4 (90 mg/kg). IV infection with A. fumigatus ATCC 13073 (10.sup.4 CFU/mouse) on Day 0. Treatment (2 h after infection) with CD101 as a single dose (2 mg/kg IV and IP) or daily (0.5 mg/kg BID) dosing. Survival monitored for 10 days. Same model was used for prophylaxis except CD101 was dosed on Days −1, −3 or −5.
[0305] Pulmonary aspergillosis: ICR mice (10/grp) were made neutropenic by cyclophosphamide on Day −4 (150 mg/kg), and CPM/cortisone on Day −1 (150/175 mg/kg). Intranasal infection with A. fumigatus AF293 (10.sup.5 CFU/mouse) on Day 0. Prophylaxis CD101 as a single dose (IP; 5, 10, 20 mg/kg) or posaconazole (PO; 2 and 10 mg/kg) 1 day prior to infection. Survival monitored for 10 days.
[0306] Results
[0307] CD101 ELF concentrations reached a maximum by 4 hours and were comparable between plasma and ELF at 24 and 48 hours (
[0308] For treatment of disseminated aspergillosis, CD101 by IV/IP at 0.2, 1, or 5 mg/kg BID×5d showed a significant increase in survival compared to vehicle. Survival was comparable when given either a single 2 mg/kg or as 0.2 mg/kg BID×5d dose. For prophylaxis, a single 5 mg/kg dose given up to 5 days prior to infection showed improved survival depending on day given. Doses 0 mg/kg showed 100% survival.
[0309] In the more challenging pulmonary aspergillosis model, dose-dependent increase in survival rate was observed from a single CD101 dose given one day prior to infection. The human (400 mg) AUC equivalent of 20 mg/kg in mice showed an increase in survival relative to control. Further comparison with posaconazole at the human AUC equivalent dose of 2 mg/kg (
Example 18: High and Sustained CD101 Lung Epithelial Lining Fluid-to-Plasma Exposure Ratio from a Single Dose: Comparison to Posaconazole and Micafungin in a Mouse Pulmonary Aspergillosis Infection Model
[0310] CD101 has demonstrated in vitro potency and in vivo efficacy in mouse models of aspergillosis. The distribution of CD101 into lung ELF was studied to further substantiate this observed efficacy.
[0311] Methods
[0312] Mice were dosed with CD101 (IP; 20 mg/kg) and then sacrificed for plasma and bronchoalveolar lavage fluid (BALF) collection between 0-72 hours. Urea for plasma/BALF normalization for ELF volume were quantified using spectrophotometry. CD101 concentrations in plasma/BALF samples were measured by LC-MS/MS. Total plasma concentrations were corrected for protein binding (99.2%).
[0313] Pulmonary aspergillosis: ICR mice (10/grp) were made neutropenic by cyclophosphamide on Day −4 (150 mg/kg), and cyclophosphamide/cortisone was given on Day −1 (150/175 mg/kg). Intranasal challenge with A. fumigatus AF293 (10.sup.5 CFU/mouse) was initiated on Day 0 and prophylaxis with CD101 as a single dose (IP; 5, 10, 20 mg/kg) or posaconazole (PO; 2 and 10 mg/kg) was started 1 day prior to infection. Survival was monitored for 10 days.
[0314] Results
[0315] Maximum CD101 ELF concentrations were observed at 4 h and were comparable between plasma and ELF by 24 h post-dose as total-drug concentrations. At 72 h, mean ELF concentration (4 μg/mL) remained considerably higher than A. fumigatus MEC.sub.90 of 0.015 μg/mL (
[0316] Dose-dependent increase in survival was observed from a single prophylaxis CD101 dose. The human (400 mg) AUC equivalent of 20 mg/kg in mice showed an increase in survival relative to control. CD101 protein binding results show a higher free fraction (˜3×) in human vs mouse plasma suggesting a lower human dose may be equally protective. Further comparison with posaconazole at the human-equivalent dose of 2 mg/kg or micafungin human-equivalent dose (100 mg) of 5 mg/kg in mice suggests an advantage for CD101 with 30% survival rate compared to no survivors for posaconazole or micafungin. Only posaconazole at 10 mg/kg (5×higher than human AUC) showed a statistically-significant increase in survival rate relative to control.
Example 19: Assessment of the Efficacy of CD101 and Comparators in a Murine Model of Pulmonary Aspergillosis
[0317] The overall aim of the studies was to assess the antifungal efficacy of CD101 by intraperitoneal administration in a murine model of pulmonary aspergillosis caused by Aspergillus fumigatus strain AF293 (A. fumigatus AF293) compared to comparators posaconazole and micafungin. The primary objective of the study was to compare survival between the treatment groups. The secondary objective was to compare lung burden in vehicle and test article treated animals.
[0318] Methods
[0319] Animal strain and housing. Mice used in these studies were supplied by Charles River (Margate UK) and were specific pathogen free. The strain of mice used was ICR (also known as CD1 Mice) which is a well characterized outbred murine strain. Male mice were 11-15 g on receipt and were allowed to acclimatize for at least 7 days.
[0320] Immunosuppression. Mice were immunosuppressed on Day −4 with 150 mg/kg cyclophosphamide administered intraperitoneally (IP), and on Day −1 with 150 mg/kg cyclophosphamide IP and 175 mg/kg cortisone acetate administered subcutaneously (SC). To prevent bacterial infection due to the immunosuppression mice were given once daily 50 mg/kg ceftazidime.
[0321] Preparation of Organism and Infection. A. fumigatus strain AF293 inoculum was prepared from spore cultures grown on Sabouraud Dextrose agar (SAB) containing 50 μg/mL chloramphenicol (SABC) in vented tissue culture flasks. Following incubation for 7-10 days at 30° C., spore cultures were washed in sterile phosphate buffered saline (PBS) containing 0.05% Tween 80. Spore count was determined using a haemocytometer and spores were diluted in PBS to ˜6.9×10.sup.6 CFU/mL. Inoculum concentration was confirmed by quantitative culture onto SABC agar.
[0322] Neutropenic mice lungs were infected with 0.04 mL (0.02 mL/nare) of ˜4.17×106 CFU/mL (˜1.67×10.sup.5 CFU/mouse) of A. fumigatus AF293 by intranasal (IN) instillation under temporary 2.5% isoflurane induced anesthesia.
[0323] Preparation of Test Articles. Micafungin (Mycamine, Astellas) was provided as a 50 mg vial (Lot 02323002, expiry August 2017) and was prepared as per manufacturer's instructions by adding 5 mL saline for injection (SFI) directly into the vial to make up a 10 mg/mL stock solution. This solution was then diluted further in SFI to a working concentration of 0.5 mg/mL. The compound was administered IP at 10 mL/kg to achieve a 2 mg/kg dose. It was prepared fresh once and stored at 4° C. until required.
[0324] Posaconazole (Noxafil 40 mg/mL oral suspension, Merck Sharp & Dohme Limited) was provided as a 40 mg/mL oral suspension (Lot N00801, expiry April 2019). This suspension was then diluted further in water for infection (WFI) to a working concentration of 0.2 and 1 mg/mL. The suspension was administered orally (PO) at 10 mL/kg for 2 and 10 mg/kg doses respectively, was prepared fresh once and stored at 4° C. until required.
[0325] Vehicle and CD101 diluent was 10% DMSO/1% Tween 20 in SFI: 1 mL of Tween 20 was added to 10 mL DMSO, gently mixed and SFI added to a final volume of 100 mL. This was filter sterilized and maintained at room temperature before use for dosing or formulating CD101. The vehicle was administered IP at 10 mL/kg.
[0326] Test article CD101 stock was prepared at 6 mg/mL in 10% DMSO/1% Tween 20 diluent. A clear non particulate solution was obtained following gentle mixing. Study doses of 20 mg/kg (2 mg/mL) were prepared from the 6 mg/mL stock as required by diluting in 10% DMSO/1% Tween 20 diluent. The 6 mg/mL stock was used undiluted for the 60 mg/kg study dose. All doses were administered IP at 10 mL/kg. The study doses were kept at 4° C. until required.
[0327] Treatment. For this study, treatments were initiated on Day 1 pre infection according to treatment groups outlined in Table 22. A total of 36 mice (6/treatment group) were used in the study.
TABLE-US-00022 TABLE 22 Murine model of pulmonary aspergillosis treatment groups Test Dosing Conc. Dosage Total Mice End of Group Article Route Schedule Day mg/mL ml/kg mg/kg Dose (ICR) study~ 1 Vehicle IP Single −1 — — — — 6 10 2 Posaconazole PO Single −1 1 10 10 2 6 10 3 Posaconazole PO Single −1 0.2 10 2 2 6 10 4 Micafungin IP Single −1 0.5 10 5 5 6 10 5 CD101 IP Single −1 2 10 20 20 6 10 6 CD101 IP Single −1 6 10 60 60 6 10
[0328] General health monitoring. The mice were monitored at a frequency appropriate for their clinical condition. Mouse weights were recorded at least once daily both to ensure animals remained within ethical limits and to monitor efficacy of treatment.
[0329] Endpoints. The primary endpoint for this study was survival within agreed ethical limits (>20% weight loss, severe hypothermia <34° C., inability to reach food or drink, severe hunching). Mice were monitored by daily weight measurements with observations as frequently as clinical condition required.
[0330] Mice presenting with severe clinical deterioration were humanely euthanized using an overdose of pentobarbitone administered by IP injection following clinical assessment and the time of death was recorded. Animal carcasses were stored at −20° C. before quantitative assessment of burden.
[0331] Ten days post infection all surviving animals were weighed and had their clinical condition assessed prior to being euthanized. Final survival numbers were recorded and analysed as described below and carcasses frozen at −20° C. prior to further processing.
[0332] Lung burden. A secondary endpoint for the study was terminal lung tissue burden. Immediately following confirmation of death, carcasses were frozen at −20° C. prior to tissue dissection and processing. The frozen carcasses were thawed at room temperature, the lungs removed and placed into pre-weighed bead-beating tubes containing 2 mL of PBS and subjected to mechanical disruption. Organ homogenates were diluted further in PBS and quantitatively cultured for A. fumigatus onto SABC and incubated at 30° C. for 24-48 hours.
[0333] In addition, a 300 μL aliquot of the undiluted lung tissue homogenate was stored at −80° C. for possible optional assessment of burden by qPCR.
[0334] Statistical analysis. Data were analysed using StatsDirect software (version 2.7.8):
[0335] 1. Survival data were analysed using the Kaplan Meier and Log-Rank and Wilcoxon tests (using the Peto-Prentice weighting method).
[0336] 2. Lung tissue burden data were analysed using the non-parametric Kruskal-Wallis test and if this was statistically significant all pairwise comparisons were analyzed (Conover-Inman).
[0337] Results
[0338] The aim of this study was to determine the in vivo efficacy of CD101 and comparators in a murine model of pulmonary aspergillosis. The design of this study is summarized in Table 22. All treatments were well tolerated with no adverse signs observed.
[0339] Body weights. Animal weights following infection with A. fumigatus AF293 are shown in
[0340] Weights remained stable up to Day 1 pre-infection. Mice from all treatment groups lost weight following the immunosuppression on Day −1. The weight loss continued after the infection in almost all treatments groups up to Day 5 post infection; thereafter any mice that survived gained weight.
[0341] Survival. The median and mean survival for the various treatments are shown in Table 23, the survival plots in
[0342] A robust survival model of pulmonary aspergillosis infection with A. fumigatus AF293 was established, with vehicle treated mice having a mean survival time of ˜77 h and a median survival time of ˜75 h post infection (range 74-80 h post infection). The study was terminated 10 days post infection as most mice had succumbed to the infection except in the 10 mg/kg posaconazole treatment group.
[0343] Treatment with test articles showed the following. [0344] 20 mg/kg CD101 dosed IP once on 1 day pre-infection—Mice had a longer mean survival time of ˜130 h compared to the vehicle treated mice but a similar median survival time of ˜75 h post infection (range 70-240 h). However, this was not statistically better than vehicle treated mice (
[0348] Posaconazole dosed at 10 mg/kg PO once on Day 1 pre-infection—Mice had a much longer mean survival time of 212 h post infection and median survival that could not be estimated as 5 mice survived to the end of the study (range 69-240 h). Statistically this was better than vehicle treated mice using the both the log-rank test and the generalized Wilcoxon test (
TABLE-US-00023 TABLE 23 Mean and median survival per treatment group Median Mean Survival Survival Treatment (Hours) (Hours) Vehicle IP 75.3 77.4 Posaconazole 10 mg/kg PO cannot estimate 211.5 Posaconazole 2 mg/kg PO 69.0 77.5 Micafungin 5 mg/kg IP 80.0 92.0 CD101 20 mg/kg IP 74.7 130.4 CD101 60 mg/kg IP 88.7 122.7
TABLE-US-00024 TABLE 24 Log-Rank and Wilcoxon test output for different comparisons Wilcoxon Comparison Log-Rank (Peto-Prentice) Vehicle vs. Posaconazole 10 mg/kg P = 0.0182 P = 0.0441 Vehicle vs. Posaconazole 2 mg/kg NS P = 0.0391 Vehicle vs. Micafungin 5 mg/kg NS NS Vehicle vs.CD101 20 mg/kg NS NS Vehicle vs. CD101 60 mg/kg NS NS NS-not significant
[0349] A small satellite study looking at the effect of immunosuppression (n=6 mice) was running with one week delay and a different batch of mice. Two mice in the study were lost several days after the Day −1 combination immunosuppression (cyclophosphamide and cortisone acetate), the remaining four mice in the study survived to the end of the study. The loss of the two mice was most likely due to secondary infection due to Pseudomonas aeruginosa, the source of which is not clear.
[0350] The main study data are unlikely to be affected by secondary infections as the positive control included, posaconazole, showed good efficacy against the infection in line with expectations based on previous results.
[0351] Lung Burden
[0352] Terminal lung burden is shown in Table 25 and
TABLE-US-00025 TABLE 25 Lung burden Group Log.sub.10 Group Log.sub.10 reduction Geometric Standard Geometric from vehicle mean Deviation mean control Treatment (CFU/g) (CFU/g) (CFU/g) (CFU/g) Vehicle IP Day −1 1.48 × 10.sup.4 1.24 × 10.sup.4 4.17 0.00 Posaconazole 10 mg/kg PO Day −1 2.75 × 10.sup.3 1.15 × 10.sup.4 3.44 0.73 Posaconazole 2 mg/kg PO Day −1 1.14 × 10.sup.4 6.17 × 10.sup.3 4.06 0.11 Micafungin 5 mg/kg IP Day −1 6.61 × 10.sup.3 7.34 × 10.sup.3 3.82 0.35 CD101 20 mg/kg IP Day −1 4.37 × 10.sup.3 1.60 × 10.sup.4 3.64 0.53 CD101 60 mg/kg IP Day −1 1.38 × 10.sup.4 2.30 × 10.sup.4 4.14 0.03
Conclusion
[0353] In this model of pulmonary aspergillosis, mice developed a robust infection with vehicle treated mice succumbing to the infection by Day 4 post infection. CD101 administered at 20 and 60 mg/kg once one day pre-infection resulted in slight increase in survival, which was statistically longer than the vehicle treatment. The comparator micafungin dosed at 5 mg/kg once one day pre-infection did not show any improvement in survival, with all mice succumbing to the infection by Day 7 post infection. The comparator posaconazole dosed at 2 mg/kg once one day pre-infection did not show any improvement in survival compared to the vehicle mice, with all mice succumbing to the infection by Day 6 post infection. Increasing the dose of posaconazole to 10 mg/kg and dosed once 1 day pre-infection resulted in >80% mice surviving to the end of the study, significantly longer than the vehicle control treatment.
OTHER EMBODIMENTS
[0354] All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each independent publication or patent application was specifically and individually indicated to be incorporated by reference.
[0355] While the invention has been described in connection with specific embodiments thereof, it will be understood that it is capable of further modifications and this application is intended to cover any variations, uses, or adaptations of the invention following, in general, the principles of the invention and including such departures from the present invention that come within known or customary practice within the art to which the invention pertains and may be applied to the essential features hereinbefore set forth, and follows in the scope of the claims.
[0356] Other embodiments are within the claims.