Dosing regimens for treatment of fungal infections

Abstract

The disclosure features pharmaceutical compositions, methods, and kits featuring dosing regimens and CD101, or a pharmaceutical acceptable salt or neutral form thereof (e.g., CD101 acetate).

Claims

1. A method of treating invasive candidiasis in a subject, wherein the method consists of: (i) (a) intravenously administering a first dose comprising 400 mg of CD101 in salt or neutral form, (b) intravenously administering a second dose comprising 200 mg of CD101 in salt or neutral form, and (c) optionally intravenously administering a third dose comprising 200 mg of CD101 in salt or neutral form, wherein the first dose is administered on day 1, the second dose is administered on day 8, and the third dose, if administered, is administered on day 15; and wherein the CD101 is administered as an aqueous pharmaceutical composition over a time period of 30 to 180 minutes or (ii) (a) intravenously administering a first dose comprising 400 mg of CD101 in salt or neutral form, (b) intravenously administering a second dose comprising 400 mg of CD101 in salt or neutral form, and (c) optionally intravenously administering a third dose comprising 400 mg of CD101 in salt or neutral form, wherein the first dose is administered on day 1, the second dose is administered on day 8, and the third dose, if administered, is administered on day 15; and wherein the CD101 is administered as an aqueous pharmaceutical composition over a time period of 30 to 180 minutes.

2. The method of claim 1, wherein the third dose is administered if on day 15 mycological eradication and/or clinical cure is not achieved in the subject or if on day 15 the subject displays symptoms of a fungal infection.

3. The method of claim 1, wherein the CD101 salt is CD101 acetate.

4. The method of claim 1, wherein the invasive candidiasis is candidemia.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 are bar graphs showing the PK-PD target attainment for the two CD101 dosing regimens, stratified by week and Minimum Inhibitory Concentration (MIC).

(2) FIG. 2 is a bar graph showing kidney burdens in mice infected with different inoculum densities of azole-resistant C. albicans strain R357.

(3) FIG. 3 shows an outline of the experimental protocol used to evaluate the efficacy of CD101, amphotericin B, and fluconazole in a C. albicans R357 infection model.

(4) FIGS. 4A and 4B are bar graphs showing effects of CD101, amphotericin B (AM-B), and fluconazole (FLU) on kidney burdens in mice infected with azole-resistant C. albicans strain R357.

(5) FIG. 5 is a scatter-plot showing PK of CD101 over doses 1 mg/kg, 4 mg/kg, and 16 mg/kg.

(6) FIG. 6 is a scatter-plot showing net change in fungal density (log.sub.10 CFU) versus different total doses of CD101 at different fractionation schedules.

(7) FIG. 7 is a bar graph showing change in fungal density (log.sub.10 CFU) reduction from baseline caused by 2 mg/kg total dose of CD101 at different fractionation schedules.

(8) FIG. 8 is a line graph showing simulated free-drug concentration time profiles relative to the MIC for the fractionated CD101 2 mg/kg regimen.

(9) FIG. 9 is a graph showing percent survival over time in mice infected with Aspergillus fumigatus and treated with 2 mg/kg CD101 (IV or IP).

(10) FIG. 10 is a table showing the activity of various antifungal agents against Candida auris clinical isolates.

DETAILED DESCRIPTION

(11) Provided are methods of treating a fungal infection in a subject in need thereof by administering to the subject an intravenous infusion of CD101, in salt or neutral form, formulated as an aqueous composition.

(12) CD101

(13) CD101 is a semi-synthetic echinocandin that inhibits the synthesis of 1,3-β-D-glucan, an essential component of the fungal cell wall of yeast forms of Candida species and regions of active cell growth of Aspergillus hyphae. The synthesis of 1,3-β-D-glucan is dependent upon the activity of 1,3-β-D-glucan synthase, an enzyme complex in which the catalytic subunit is encoded by FKS1, FKS2, and FKS3 genes. Inhibition of this enzyme results in rapid, concentration-dependent, fungicidal activity for Candida spp. The structure of CD101 is depicted above.

(14) Therapy

(15) The treatment regimens and pharmaceutical compositions described herein can be used to treat or prevent fungal infections.

(16) The fungal infection being treated can be an infection selected from tinea capitis, tinea corporis, tinea pedis, onychomycosis, perionychomycosis, pityriasis versicolor, oral thrush, vaginal candidiasis, respiratory tract candidiasis, biliary candidiasis, eosophageal candidiasis, urinary tract candidiasis, systemic candidiasis, mucocutaneous candidiasis, mucormycosis, paracoccidioidomycosis, North American blastomycosis, histoplasmosis, coccidioidomycosis, sporotrichosis, fungal sinusitis, or chronic sinusitis. For example, the infection being treated can be an infection by a Candida species (e.g., C. albicans, C. glabrata, C. dubliniensis, C. krusei, C. parapsilosis, C. tropicalis, C. orthopsilosis, C. guilliermondii, C. rugosa, C. auris, C. lusitaniae, or other Candida species).

(17) In some embodiments, a fungal infection can be an antifungal 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 fungus (e.g., an antifungal drug-resistant strain of Candida spp.)). Antifungal drugs include, but are not limited to, azole compounds, echinocandins, polyene compounds, and flucytosine.

(18) For example, an echinocandin-resistant fungal infection refers to a fungal infection that is refractory to treatment with an echinocandin. In such infections the fungus that causes the infection is resistant to treatment with one or more echinocandins. The one or more echinocandins are cyclic lipopeptides that inhibit the synthesis of glucan in the cell wall by inhibition of the 1,3-β-D-glucan synthase enzyme complex. The one or more echinocandins referred to in the term “echinocandin-resistant fungal infection” include micafungin, caspofungin, and anidulafungin, but does not include CD101, in salt or neutral form. Thus, using the methods of the disclosure, CD101, in salt or neutral form, can be used to treat micafungin-resistant, caspofungin-resistant, and/or anidulafungin-resistant fungal infections.

(19) An antifungal drug-resistant fungal infection may also be an azole-resistant fungal infection, which refers to a fungal infection that is refractory to treatment with an azole compound. In such infections the fungus that causes the infection is resistant to treatment with one or more azole compounds. The azole compounds referred to in the term “azole-resistant fungal infection” are antifungal compounds that contain an azole group, which is a five-membered heterocyclic ring having at least one N and one or more heteroatoms selected from N, O, or S. Antifungal azole compounds function by binding to the enzyme 14α-demethylase and disrupt, inhibit, and/or prevent its natural function. The enzyme 14α-demethylase is a cytochrome P450 enzyme that catalyzes the removal of the C-14 α-methyl group from lanosterol before lanosterol is converted to ergosterol, an essential component in the fungal cell wall. Therefore, by inhibiting 14α-demethylase, the synthesis of ergosterol is inhibited. Examples of azole compounds include, but are not limited to, VT-1161, VT-1598, fluconazole, albaconazole, bifonazole, butoconazole, clotrimazole, econazole, efinaconazole, fenticonazole, isavuconazole, isoconazole, itraconazole, ketoconazole, luliconazole, miconazole, omoconazole, oxiconazole, posaconazole, pramiconazole, ravuconazole, sertaconazole, sulconazole, terconazole, tioconazole, and voriconazole.

(20) An antifungal drug-resistant fungal infection may also be a polyene-resistant fungal infection, which refers to a fungal infection that is refractory to treatment with a polyene compound. In such infections, the fungus that causes the infection is resistant to treatment with one or more polyene compounds. Polyene compounds are compounds that insert into fungal membranes, bind to ergosterol and structurally related sterols in the fungal membrane, and disrupt membrane structure integrity, thus causing leakage of cellular components from a fungus that causes infection. Polyene compounds typically include large lactone rings with three to eight conjugated carbon-carbon double bonds and may also contain a sugar moiety and an aromatic moiety. Examples of polyene compounds include, but are not limited to, 67-121-A, 67-121-C, amphotericin B, arenomvcin B, aurenin, aureofungin A, aureotuscin, candidin, chinin, demethoxyrapamycin, dermostatin A, dermostatin B, DJ-400-B.sub.1, DJ-400-B.sub.2, elizabethin, eurocidin A, eurocidin B, filipin I, filipin II, filipin III, filipin IV, fungichromin, gannibamycin, hamycin, levorin A.sub.2, lienomycin, lucensomycin, mycoheptin, mycoticin A, mycoticin B, natamycin, nystatin A, nystatin A.sub.3, partricin A, partricin B, perimycin A, pimaricin, polifungin B, rapamycin, rectilavendomvcin, rimocidin, roflamycoin, tetramycin A, tetramycin B, tetrin A, and tetrin B.

(21) An antifungal drug-resistant fungal infection may also be a flucytosine-resistant fungal infection, which refers to a fungal infection that is refractory to treatment with the synthetic antifungal drug flucytosine. A brand name for flucytosine is Ancobon®.

(22) A Candida infection can be caused by an antifungal drug-resistant strain of fungus in the genus Candida, such as an antifungal drug-resistant strain of C. albicans, C. parapsilosis, C. glabrata, C. guilliermondii, C. krusei, C. lusitaniae, C. auris, C. tropicalis, or other Candida species. In some embodiments, a Candida infection can be caused by an azole-resistant strain of fungus in the genus Candida, such as an azole-resistant strain of C. albicans, C. parapsilosis, C. glabrata, C. guilliermondii, C. krusei, C. lusitaniae, C. auris, C. tropicalis, or other Candida species. In some embodiments, an azole-resistant strain of fungus is Candida albicans, e.g., C. albicans R357 strain. Azole-resistant C. albicans R357 strain contains mutations in the gene ERG11 (e.g., C. albicans ERG11 (CaERG11)). The CaERG11 gene encodes the enzyme 14α-demethylase, the target of azole antifungal compounds. Mutations in the CaERG11 gene that result in amino acid substitutions alter the abilities of the azole compounds to bind to and inhibit 14α-demethylase, thus resulting in resistance. In some embodiments, an azole-resistant C. albicans R357 strain have an increase in CaERG11 expression, e.g., 2-15 times (e.g., 3-15, 4-15, 5-15, 6-15, 7-15, 8-15, 9-15, 10-15, 11-15, 12-15, 13-15, or 14-15 times) more increased expression relative to a wild-type strain. In some embodiments, an azole-resistant C. albicans R357 strain have one or more mutations in the CaERG11 gene that lead to one or more amino acid substitutions, e.g., D116E, D153E, and/or E266D. In some embodiments, an azole-resistant Candida albicans R357 strain have no significant changes in CDR1 or MDR1 expression. Table 1 shows the percentage of inhibition and MIC values of three azole compounds, amphotericin B, caspofungin, and CD101 towards the azole-resistant C. albicans R357 strain and susceptibility status (S: susceptible; R: resistant) as classified by CLSI (Clinical and Laboratory Standards Institute) of the C. albicans R357 strain towards the listed compounds.

(23) TABLE-US-00001 TABLE 1 Antifungal Endpoint MIC agent (% inhibition) (μg/mL) Susceptibility (CLSI) Fluconazole 50% >64 R Voriconazole 50% >64 R Posaconazole 50% >64 Amphotericin B 100% 0.5 S Caspofungin 50% 0.25 S CD101 50% 0.125

(24) Clinical isolates of C. auris that may be treated or prevented by the treatment regimens and pharmaceutical compositions described herein are described in the Examples section (e.g., Example 9) 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 2.

(25) TABLE-US-00002 TABLE 2 # 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/14 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/14 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/14 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/14 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/14 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/14 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

(26) The treatment regimens and pharmaceutical compositions described herein can be administered to prevent a fungal infection in a subject in need thereof. For example, subjects may receive prophylaxis treatment 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. 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 liver infections) in a subject.

(27) The following examples are put forth so as to provide those of ordinary skill in the art with a complete disclosure and description of how the methods and compounds claimed herein are performed, made, and evaluated, and are intended to be purely exemplary of the disclosure and are not intended to be limiting.

EXAMPLES

Example 1

Administration of CD101 to Healthy Adult Subjects

(28) Clinical studies have shown that CD101 is safe and well tolerated as a single dose up to 400 mg and multiple doses up to 400 mg.

(29) In a first study, CD101 was administered by IV injection to healthy adult subjects. In this study, subjects in 4 cohorts of 8 subjects (6 active, 2 placebo) each were randomized to receive single IV doses of CD101 or placebo (normal saline) infused over 60 (±5) minutes. Dose levels of CD101 assessed follow an ascending single-dose regimen (50, 100, 200, or 400 mg).

(30) A total of 32 subjects were randomized, with 31 subjects completing all study assessments. One subject prematurely withdrew for personal reasons unrelated to safety or tolerability. Subjects were primarily White (97%), Hispanic (94%), and males and females were approximately equally represented (53% and 47%, respectively). There were no serious adverse events (SAEs), severe adverse events (AEs), or dose-response relationships for overall AEs. The majority of AEs were mild, and all AEs completely resolved by the end of the study. There were no drug-related AEs resulting from clinically significant hematology or clinical chemistry laboratory abnormalities at any dose. In addition, there were no safety issues related to electrocardiograms (ECGs), vital signs, or physical exam findings.

(31) A second study of CD101 administered by IV injection to healthy adult subjects was also performed. In this study, subjects in 3 cohorts of 8 subjects (6 active, 2 placebo) each were randomized to receive multiple IV doses of CD101 or placebo (normal saline) infused over 60 (±5) minutes. Dose levels of CD101 assessed follow an ascending multiple-dose regimen (100 mg×2 doses, 200 mg×2 doses, or 400 mg×3 doses).

(32) A total of 24 subjects were randomized and all subjects completed the study. Subjects were primarily White (88%), Hispanic or Latino (88%), and had a mean body mass index (BMI) of 27.208 kg/m.sup.2 and a mean age of 42.8 years. Males and females were equally represented (50% each). There were no SAEs or severe AEs. The majority of AEs were mild, and all related AEs completely resolved by the end of the study. Four subjects in the CD101 group experienced mild, transient infusion reactions, characterized by flushing, sensation of warmth, nausea, and chest tightness. These infusion reactions were associated primarily with the 400 mg dose cohort and were most common with the third dose. These reactions occurred within minutes of infusion initiation and disappeared within minutes without interruption or discontinuation of the study drug infusion. There were no drug-related AEs resulting from clinically significant hematology or clinical chemistry laboratory abnormalities at any dose. In addition, there were no safety issues related to ECGs, vital signs, or physical exam findings.

Example 2

Clinical Pharmacology of CD101

(33) As is described below, the pharmacokinetics of CD101 have been well-characterized in healthy subjects for doses up to 400 mg for 3 weeks.

(34) Single Ascending Dose Pharmacokinetics

(35) Pharmacokinetics were first determined by analyzing plasma and urine samples for concentration of CD101 obtained from subjects who received CD101 in each cohort at various time points after administration of the single dose of the study drug.

(36) The plasma PK of CD101 was generally well-characterized following the 50, 100, 200, and 400 mg CD101 doses. Exposure to CD101 increased with increasing CD101 doses (Table 3). Time to reach C.sub.max (i.e., T.sub.max) was observed at the end of infusion, as expected, at approximately 1 hour after the start of infusion for all doses. Elimination of CD101 appears multiphasic. AUC and C.sub.max increased in a dose proportional manner and total body clearance was similar throughout the dose levels with t.sub.1/2 values of >80 hours through the first week of plasma collection (a longer terminal t.sub.1/2 of 127-146 hours is calculated when incorporating data from later collection times). Total body clearance was approximately 4 mL/min across the CD101 doses, indicating linear kinetics for CD101 across the doses investigated. Volume of distribution (V.sub.z and V.sub.ss) ranged from 33 to 48 L. The fraction of dose excreted in urine was <1% at all dose levels, indicating minor contribution of renal clearance in CD101 excretion.

(37) TABLE-US-00003 TABLE 3 Summary of Plasma CD101 Exposures Following Administration of 50, 100, 200, and 400 mg 1-hour Intravenous Infusion of CD101 Dose C.sub.max C.sub.144 AUC.sub.0-168 t.sub.1/2 (mg) (μg/mL) (μg/mL) (μg .Math. h/mL) (hours) 50 2.76 0.481 145 86 100 4.84 0.854 254 92 200 10.9 2.01 592 91 400 22.7 3.83 1160 84 AUC.sub.0-168 = area under the curve from time 0 to 168 hours; C.sub.144 = plasma concentration at 144 hours post start of infusion; C.sub.max = maximum plasma concentration; t½ = half-life.

(38) Multiple Ascending Dose Pharmacokinetics

(39) Pharmacokinetics were determined by analyzing plasma and urine samples for concentration of CD101 obtained from subjects who received CD101 in each cohort at various time points after administration of CD101.

(40) The plasma PK of CD101 was also well characterized following 2 or 3 weekly doses of CD101: 100 mg (Day 1/Day 8), 200 mg (Day 1/Day 8), and 400 mg (Day 1/Day 8/Day 15). Exposures following the first dose were very comparable to that observed in the SAD study, with AUC and C.sub.max generally increasing in a dose proportional manner (Table 4). Accumulation was minor, ranging from 14% to 34% (or 1.14 to 1.34) as measured by C.sub.max ratio of last/first dose and 30% to 55% (or 1.30 to 1.55), as measured by the AUC.sub.0-168 ratio of last/first dose.

(41) TABLE-US-00004 TABLE 4 Summary of Plasma CD101 Exposures Following Administration of 100 mg (Day 1/Day 8), 200 mg (Day 1/Day 8), and 400 mg (Day 1/Day 15) Weekly 1-hour Intravenous Infusion of CD101 Dose C.sub.max AUC.sub.0-168 Accumulation Ratio (mg) Day (μg/mL) (μg .Math. h/mL) C.sub.max AUC.sub.0-168 100 1 5.67 299 1.14 1.30 8 6.49 390 200 1 10.6 570 1.17 1.43 8 12.4 813 400 1 22.7 1190 1.34 1.55 15 30.5 1840 AUC.sub.0-168 = area under the curve from time 0 to 168 hours; C.sub.max = maximum plasma concentration.

(42) Data from the above studies were used to develop a population PK model to describe the time course of CD101 concentrations after IV administration of single and multiple, once-weekly doses. In brief, the data were best described using a 4-compartment model with 0-order drug input via the IV infusion and first-order, linear elimination. In order to account for the relationships between the structural PK parameters and subject body weight, all parameters in the model were scaled to subject body weight using standard allometric coefficients (a power of 0.75 for the clearance terms and 1.0 for the volume terms). This model fit the observed data with very little bias and excellent precision.

(43) Monte Carlo simulations were conducted to assess the probability of PK-pharmacodynamic (PD) target attainment using a variety of exploratory dosing regimens. Two dosing regimens were selected for further investigation (Table 5). The weekly free-drug area under the CD101 concentration-time curve from time 0 to 168 hours (fAUC.sub.0-168) after each dose was simulated for 2000 hypothetical patients; patient body weight was simulated using a database of patient demographic characteristics and plasma protein binding was assumed to be 99.1%. Nonclinical studies of Candida albicans infections in mice have shown that a CD101 fAUC.sub.0-168:MIC ratio of 10 has been associated with a 2-log reduction in fungal burden in infected kidneys. This value of 10 was therefore chosen as the PK-PD target of interest for the Monte Carlo simulations.

(44) Two regimens (400 mg/400 mg/400 mg and 400 mg/200 mg/200 mg) are predicted to provide adequate PK-PD target attainment up to a MIC of 0.5 mg/L (3 dilution steps higher than the MIC.sub.90 of 0.06 for C. albicans and glabrata based upon surveillance data from Sentry 2014). Additionally, due to the accumulation with repeated doses, the 400 mg IV once weekly regimen would be expected to achieve higher PK-PD target attainment at an MIC of 1 mg/L in Weeks 2 and 3 of therapy, and thus is expected to provide additional benefit beyond the first week of therapy against pathogens with an MIC ≥1 mg/mL. The PK-PD target attainment for the 2 chosen regimens are shown in Table 5 and FIG. 1.

(45) TABLE-US-00005 TABLE 5 Predicted Pharmacokinetic-Pharmacodynamic Target Attainment for CD101 Regimens, Stratified by Week and Minimum Inhibitory Concentration MIC (mg/L).sup.b Regimen.sup.a Week 0.06 0.12 0.25 0.5 1 2 400/400/400 1 100 100 100 99.4 46.6 0.10 2 100 100 100 100 86.3 2.60 3 100 100 100 100 93.8 6.85 400/200/200 1 100 100 100 100 47.3 0.05 2 100 100 100 97.4 14.7 0 3 100 100 100 97.2 14.0 0 MIC = minimum inhibitory concentration. .sup.aRegimens defined by the weekly dose (e.g., 400/200/200 represents 400 mg for the first dose followed by 200 mg IV once weekly for two doses). .sup.bItalicized text indicates PK-PD target attainment above 90%.

Example 3

Treatment of Subjects With Candidemia and/or Invasive Candidiasis

(46) Subjects with candidemia and/or invasive candidiasis receive CD101 Injection (400 mg on each of Day 1 and Day 8, with an optional dose of 400 mg on Day 15; or 400 mg on each of Day 1, Day 8, and Day 15, with an optional dose of 400 mg on Day 22; or 400 mg on each of Day 1, Day 8, Day 15, and Day 22, with an optional dose of 400 mg on Day 29; or 400 mg on each of Day 1, Day 8, Day 15, Day 22, and Day 29, with an optional dose of 400 mg on Day 36; or 400 mg on Day 1 and 200 mg on Day 8, with an optional dose of 200 mg on Day 15; 400 mg on Day 1 and 200 mg on each of Day 8 and Day 15, with an optional dose of 200 mg on Day 22; 400 mg on Day 1 and 200 mg on each of Day 8, Day 15, and Day 22, with an optional dose of 200 mg on Day 29; 400 mg on Day 1 and 200 mg on each of Day 8, Day 15, Day 22, and Day 29, with an optional dose of 200 mg on Day 36). Mycological diagnosis of candidemia and/or invasive candidiasis is established by ≥1 blood culture positive for Candida spp. within 96 hours from time of collection before administration of the first dose.

(47) CD101 is supplied as a sterile solution or as a lyophilized formulation. Vials of CD101 Injection are diluted with normal saline in an infusion bag. CD101 is administered by IV infusion over 60 (±5) minutes on day 1, day 8, and optionally, day 15.

(48) In some embodiments, CD101 Injection is provided as a sterile aqueous or lyophilized product for dilution (e.g., in sodium chloride 0.9%) prior to infusion. In some embodiments, one or more vials of aqueous CD101 are diluted in infusion bags.

(49) CD101 is administered over a time period of 30 to 180 minutes (e.g., over 30±5 minutes, 60±5 minutes, 90±5 minutes, 120±5 minutes, 150±5 minutes, 180±5 minutes, 30±10 minutes, 60±10 minutes, 90±10 minutes, 120±10 minutes, 150±10 minutes, or 180±10 minutes).

Example 4

Assessment of Infection Following Azole-Resistant Candida albicans R357 Infection

(50) The azole-resistant C. albicans R357 was obtained from a frozen working stock and thawed at room temperature. A 0.1 mL aliquot of the stock was transferred to a sabouraud agar (SA) plate and incubated at 35-37° C. overnight. The culture was re-suspended in 1 mL cold PBS (>2.0×10.sup.9 CFU/mL, OD.sub.6203.0-3.2) and diluted with PBS to target inoculum sizes of 5×10.sup.6, 5×10.sup.5, 5×10.sup.4, and 5×10.sup.3 CFU/mL. The actual colony counts were determined by plating dilutions to SA plates followed by 20-24 hr incubation.

(51) Groups of male ICR (Institute of Cancer Research) mice (n=3 per group) weighing 22±2 g were used. Immune suppression was induced by two intraperitoneal injections of cyclophosphamide at 150 mg/kg 4 days (Day—4) and at 100 mg/kg 1 day (Day—1) before C. albicans infection. On Day 0, animals were intravenously inoculated (0.2 mL/mouse) with the R357 suspension. The animals were euthanized by CO.sub.2 asphyxiation at 2 and 72 hr post-inoculation. A summary of the experimental design is shown in Table 6.

(52) TABLE-US-00006 TABLE 6 Experimental Design Inoculum size Time at sacrifice ICR Mice Group (CFU/animal) Post-infection (male) 1a 1E6  2 hr 3 1b 1E6 72 hr 3 2a 1E5  2 hr 3 2b 1E5 72 hr 3 3a 1E4  2 hr 3 3b 1E4 72 hr 3 4a 1E3  2 hr 3 4b 1E3 72 hr 3

(53) Paired kidneys were harvested and weighed. The harvested kidneys were homogenized in 1 mL sterile PBS (pH 7.4) and 10-fold dilutions were prepared and separately plated onto SA plates for further 20-24 hr incubation and then the fungal counts (CFU/g) in kidneys were calculated. Kidney fungal burdens from different inoculum densities of azole-resistant C. albicans strain R357 are shown in FIG. 2.

Example 5

Efficacy of Amphotericin B, Fluconazole, and CD101 in the Disseminated Infection Model with C. albicans R357

(54) Materials

(55) Test Articles. CD101 was dissolved in the vehicle containing 10% DMSO and 1% Tween 20 in 0.9% NaCl (see formulation table below). Amphotericin B and fluconazole were in powder form. Amphotericin B was dissolved in 0.9% NaCl. Fluconazole was dissolved in water (WFI: water for injection). A summary of the test articles is shown in Table 7.

(56) TABLE-US-00007 TABLE 7 Test Articles Light Formulation Test Article Vehicle Solubility.sup.a Color Protection.sup.b Temp. mg/mL CD101 10% DMSO/1% S colorless- Yes 4° C. 0.3, 1 and 3     Tween 20 in 0.9% NaCl Amphotericin B 0.9% NaCl S light yellow Yes 4° C. 0.1 and 0.3 Fluconazole WFI S colorless Yes RT 2 .sup.aThis is based on visual observation (S: soluble; SS: slightly soluble; I: insoluble (suspension or precipitation). .sup.bTest article is kept in tube or vial with brown color, or covered with aluminum foil. c: 4° C.: prepared fresh and stored in the refrigerator or kept on ice; ET: prepared fresh and stored between 20-25° C.

(57) Organism. The C. albicans strains R357 was cryopreserved as single-use frozen working stock cultures stored at −70° C.

(58) Animals. Male ICR mice weighing 22±2 g were acclimated for 3 days prior to use and were confirmed to be in good health. Space allocation for 3 or 5 animals was 27×20×14 cm. All animals were maintained in a hygienic environment with controlled temperature (20-24° C.), humidity (30%-70%) and 12 hours light/dark cycles. Free access to sterilized standard lab diet and autoclaved tap water were granted. All aspects of this work including housing, experimentation, and animal disposal were performed in general accordance with the “Guide for the Care and Use of Laboratory Animals: Eighth Edition” (National Academies Press, Washington, D.C., 2011).

(59) Chemicals. Amphotericin B powder (Cat #A-9528, Sigma, USA), Bacto agar (Cat #214040, BD DIFCO, USA), cyclophosphamide (Cat #C-0768, Sigma, USA), dimethyl sulfoxide (Cat #1.02931.1000, Merck, Germany), fluconazole powder (Cat #F8929, SIGMA-Aldrich, USA), Fluid Sabouraud medium (Cat #264210, BD DIFCO, USA), Phosphate buffer saline (PBS) (Cat #P4417, Sigma, USA), Sodium chloride (Cat #S7653, SIGMA-Aldrich, USA), Tween 20 (Cat #P-7949, Sigma, USA) and Water for injection (WFI) (Tai-Yu, Taiwan).

(60) Equipment. Biological safety cabinet (NuAire, USA), Absorbance microplate readers (Tecan, Infinite F50, USA), Centrifuge (Model 5922, Kubota, Japan), Individually Ventilated Cages (IVC, 36 Mini Isolator systems) (Tecniplast, Italy), Laminar flow (Tsao-Hsin, Taiwan), Orbital shaking incubator (Firstek Scientific, Taiwan), Pipetman (Rainin, USA), Polytron homogenizer (Kinematica, Switzerland) and Ultra-Low temperature freezer (NuAire, USA).

(61) Methods

(62) The azole-resistant C. albicans (R357) strain was obtained from a frozen working stock and thawed at room temperature. A 0.1 mL aliquot stock was transferred to a sabouraud agar (SA) plate and incubated at 35-37° C. overnight. The culture was re-suspended in 1 mL cold PBS (>2.0×10.sup.9 CFU/mL, OD.sub.620 3.0-3.2) and diluted with PBS to 5×10.sup.5 CFU/mL. The actual colony counts were determined by plating dilutions to SA plates followed by 20-24 hr incubation. The actual inoculum count was 7.05×10.sup.5 CFU/mL.

(63) Groups of male ICR mice (n=5 per group) weighing 22±2 g were used. Immune suppression was induced by two intraperitoneal injections of cyclophosphamide at 150 mg/kg 4 days (Day—4) and at 100 mg/kg 1 day (Day—1) before C. albicans infection. On Day 0, animals were intravenously inoculated (0.2 mL/mouse) with 5 inoculum sizes at 1.41×10.sup.5 CFU/0.2 mL/mouse of C. albicans (R357). CD101 was administered by intraperitoneal (IP) injection at 3, 10 and 30 mg/kg. Amphotericin B (AM-B) was administered by intravenous (IV) injection at 1 and 3 mg/kg. Fluconazole (FLU) was administered by oral gavage (PO) at 20 mg/kg. All test articles were administered once 2 hours after inoculation. The dosing volume was 10 mL/kg for all groups. A summary of the experimental design is shown in Table 8.

(64) TABLE-US-00008 TABLE 8 Experimental Design Animal Dose Conc. Dosage ICR Mice Group Test Article Sacrifice Route mg/mL mL/kg mg/kg (male) 1 N/A  2 hr — — — — 5 2 Vehicle 72 hr IP — 10 — 5 3 Vehicle 48 hr IP — 10 — 5 4 Amphotericin B 72 hr IV 0.1 10 1 5 5 Amphotericin B 48 hr IV 0.1 10 1 5 6 Amphotericin B 72 hr IV 0.3 10 3 5 7 Amphotericin B 48 hr IV 0.3 10 3 5 8 Fluconazole 72 hr PO 2 10 20 5 9 Fluconazole 48 hr PO 2 10 20 5 10 CD101 72 hr IP 0.3 10 3 5 11 CD101 48 hr IP 0.3 10 3 5 12 CD101 72 hr IP 1 10 10 5 13 CD101 48 hr IP 1 10 10 5 14 CD101 72 hr IP 3 10 30 5 15 CD101 48 hr IP 3 10 30 5 Target inoculum size 1E05 CFU/mouse (the actual inoculum size was 1.41E05 CFU/mouse). Vehicle: 10% DMSO/1% Tween 20 in 0.9% NaCl Test articles were dosed once 2 hrs after infection. Animals were sacrificed at assigned time points after infection.

(65) The animals were euthanized by CO.sub.2 asphyxiation 48 and 72 hr post-inoculation. Paired kidneys were harvested and weighed. The harvested kidneys were homogenized in 1 mL sterile PBS (pH 7.4) and 10-fold dilutions were prepared and separately plated onto SA plates. The fungal counts (CFU/g) in kidneys were calculated and the decrease percentage was calculated by the following formula:
Decrease (%)=[(CFU/g of vehicle−CFU/g of treatment)/(CFU/g of vehicle)]×100%

(66) An outline of the experimental protocol is shown in FIG. 3. FIGS. 4A and 4B show the absolute fungal counts and the difference in fungal counts, respectively, of the test article treatment groups measured 48 or 74 hr after infection. A decrease of 99% or more (≥99%, 2-log) in the fungal counts of treated animals compared to those in the vehicle group measured 48 or 72 hr after infection indicated significant antimicrobial activity. One-way ANOVA followed by Dunnett's test was also applied to assess statistical significance.

(67) Significant antimicrobial effects (P<0.05) were observed with CD101 treatment groups at 3, 10, and 30 mg/kg IP at 48 and 72 hr after infection. A two log reduction in fungal counts was observed with all CD101 treatment groups at the 48 and 72 hr time points. Significant effects were observed following amphotericin B treatment at 1 and 3 mg/kg IV at 48 and 72 hr after infection. Amphotericin B treatment at 3 mg/kg IV resulted in a two log reduction in counts at 72 hr time point. Administration of fluconazole at 20 mg/kg PO elicited a moderate reduction (51% and 84%) in colony counts 48 and 72 hr after infection compared to the vehicle control group that was not significant with one-way ANOVA followed by Dunnett's test analysis (P>0.05).

Example 6

Pharmacological Basis of CD101 Efficacy

(68) Methods

(69) Pharmacokinetic Study. Healthy female ICR mice were given a single dose of CD101 via intraperitoneal (IP) injection. The following doses, at three mice per dose, were studied: 1, 4, and 16 mg/kg. CD101 plasma concentrations were determined at 0, 1, 3, 6, 12, 24, 48, 72, 96 hours post-dose using a validated LC/MS assay with a lower limit of quantification of 0.02 μg/mL.

(70) Dose-Fractionation Study. Male or female ICR mice (5 per regimen and observation time) weighing 22±2 g were rendered neutropenic for the study by injecting the mice with cyclophosphamide treatment four days (—Day 4) (150 mg/kg IP) and one day (—Day 1) prior to infection at 100 mg/kg IP. Neutropenia was sustained for the duration of the study with cyclophosphamide doses (100 mg/kg IP) every 48 hours on days +1, +3, +5 and +7 after infection. Each animal was inoculated intravenously with 1×10.sup.3 CFU of C. albicans (Strain R303, MIC=0.125 mg/L). CD101 (or vehicle) was administered 24 hours post-infection via IP injection. The doses studied are shown in Table 9.

(71) TABLE-US-00009 TABLE 9 Summary of CD101 dosing regimens evaluated Total Dose Dosing Interval Fractionated Doses 0.7 mg/kg   Single Dose 0.7 mg/kg × 1 Twice Weekly 0.35 mg/kg × 2 Daily 0.1 mg/kg × 7 2 mg/kg Single Dose 2 mg/kg × 1 Twice Weekly 1 mg/kg × 2 Daily 0.29 mg/kg × 7 7 mg/kg Single Dose 7 mg/kg × 1 Twice Weekly 3.5 mg/kg × 2 Daily 1 mg/kg × 7

(72) Mice were sacrificed 168 hours (7 days) following the start of treatment. Control arm mice were sacrificed 0, 24, and 48 hours post administration of vehicle. Paired kidneys are aseptically harvested, homogenized, and plated for colony counts to determine the fungal burden (CFU/g).

(73) Pharmacokinetic-Pharmacodynamic Analyses. Using the data collected from the PK study, a PK model was developed in S-ADAPT. Using the developed PK model, concentration-time profiles and AUC.sub.0-168h values were computed for each dosing regimen administered in the dose-fractionation study. Free-drug plasma concentrations were generated using a murine protein binding value of 99.1%. Relationships between the change in log.sub.10 CFU from start of therapy and AUC.sub.0-168h were explored.

(74) Results

(75) CD101 exhibited linear PK over the dose ranged studied (1 to 16 mg/kg IP). A 4-compartment model best described the PK data. Model fits are displayed in FIG. 5.

(76) The results of the dose-fractionation study are displayed in FIG. 6, which shows that fungi grew well in the no-treatment control group. The magnitude of net change in fungal density (log.sub.10 CFU) was similar regardless of fractionation schedule within the CD101 0.7 and 7 mg/kg dosing groups. However, results within the CD101 2 mg/kg group varied by the fractionation schedule.

(77) The change in log.sub.10 CFU reduction from baseline at 168 hours by fractionation schedule for the CD101 2 mg/kg group is displayed in FIG. 7. When a total dose of 2 mg/kg was delivered daily (0.29 mg/kg/day), the magnitude of net change in fungal density (log.sub.10 CFU) was similar to the no-treatment control group. However, when 2 mg/kg is delivered as a single dose, there was a greater than 2-log.sub.10 CFU reduction from baseline at 168 hours. The 2 mg/kg×1 and 0.29 mg/kg daily×7 regimens had similar cumulative CD101 exposures at 168 hours, as displayed in FIG. 6. Despite having similar exposures, which influences efficacy, these regimens showed very different effects.

(78) Free-drug plasma concentration-time profiles of the three fractionated CD101 2 mg/kg dosing regimens are displayed in FIG. 8. All three regimens display very different exposure profiles. In particular, the single dose regimen results in larger CD101 exposures early in therapy. Free-drug plasma AUC.sub.0-24 is 0.0654, 0.0303, and 0.00948 mg.Math.h/L following administration of CD101 2 mg/kg as a single dose, twice weekly, and daily regimen, respectively. Further, administration of a single dose results in free-drug plasma concentrations which remain above those for the twice weekly and daily regimens for 84 and 48 hours, respectively.

(79) Three CD101 regimens with similar total exposures, yet very different exposure shapes, display considerably different efficacy. This suggests that the shape of the CD101 AUC is a determinant of efficacy, with front loaded regimens demonstrating greater efficacy. The magnitude of the net change in fungal burden was similar regardless of fractionation schedule within the CD101 0.7 and 7 mg/kg dosing groups, but differed within the 2 mg/kg group. A 2 mg/kg dose was considerably more effective when given once per week compared to the same dose divided into twice-weekly or daily regimens.

Example 7

Efficacy of CD101 in Mouse Models of Aspergillosis and Azole-Resistant Disseminated Candidiasis

(80) Methods

(81) The in vivo efficacy of CD101 was evaluated using neutropenic mouse models of azole-resistant candidiasis and aspergillosis. An azole-resistant strain of C. 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.

(82) Results

(83) 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; FIG. 9).

(84) Conclusions

(85) 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. One dose of CD101 also demonstrated efficacy in the mouse model of aspergillosis. These data support the continued development of CD101 for treatment of serious infections caused by Candida, including azole-resistant strains, and Aspergillus spp.

Example 8

Efficacy of CD101 Against Candida auris Clinical Isolates

(86) Materials and Methods

(87) Organisms and Antifungal Agents

(88) 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) 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).

(89) Minimum Inhibitory Concentration (MIC) Assays

(90) Broth microdilution MIC assays performed according to CLSI M38-A2 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 by centrifugation and normal saline (0.85% NaCl) washes. 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 (FIG. 10). To check the inoculum count, ten-fold dilutions of C. auris working conidial suspension were plated onto SDA media. Inoculum plates were incubated at 37° C. for 2 days prior to determining colony count.

Example 9

Efficacy CD101, Caspofungin (CAS), Micafungin (MICA), and Fluconazole (FLU) Against Candida auris Clinical Isolates and FKS1 HS1 Sequence Analysis

(91) 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.

(92) Materials and Methods

(93) Candida auris isolates. Thirty-eight C. auris strains, obtained from VP Chest Institute, University of Delhi (Delhi, India) were used in the study (Table 10). Strains were grown on yeast extract peptone dextrose (YPD) agar plates prior to testing.

(94) TABLE-US-00010 TABLE 10 C. auris strain # 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

(95) 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).

(96) 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).

(97) Results

(98) 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 11. 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.

(99) FKS1 HS1 PCR/sequencing. Results of C. auris isolates FKS1 HS1 sequence analysis are shown in Table 11. 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 11), determined as echinocandin-resistant, exhibited serine to phenylalanine amino acid substitution in position equivalent to FKS1 HS1 S645 in Candida albicans.

(100) TABLE-US-00011 TABLE 11 In vitro antifungal susceptibility profile and FKS1 HS1 characteristics of Candida auris strains C. auris strain # CD101 CAS MICA FLU Strain # (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   >16  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 mg/L; **loss of CAS paradoxical effect, no possibility to read MIC, fungal growth reduction <50%)

(101) Conclusions

(102) 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. Echinocandin resistance 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 10

In Vivo Pharmacokinetic/Pharmacodynamic (PK/PD) Evaluation of CD101 Against C. albicans and C. glabrata

(103) Methods

(104) 4 C. albicans and 3 C. glabrata strains were used. MICs were determined by CLSI standards. Single dose plasma PK was determined in groups of three mice after IP doses of 1, 4, 16, and 64 mg/kg. For treatment studies, mice were rendered neutropenic via administration of cyclophosphamide at days −4, −1, +2 and +4. Mice were infected with 6.3±0.1 CFU/ml (C. albicans) or 6.2±0.2 CFU/ml (C. glabrata) injected into the lateral tail vein. Treatment dose range was 0.016-64 mg/kg, given once by IP injection 2 h after infection. Experiment duration was 7 days at which point kidneys were aseptically harvested for CFU counts. The Emax Hill equation was used to model the dose-response data to PK/PD index AUC/MIC. The static and 1-log kill doses, as well as associated AUC/MIC values were determined for each isolate.

(105) Results

(106) CD101 MICs were 0.008-0.06 mg/L for C. albicans and 0.06-0.5 mg/L for C. glabrata. Single dose plasma PK parameter ranges include: Cmax 2.6-77 mg/L, AUC.sub.0-∞93-4046 mg*h/L, T1/2 28-41 h. Dose-dependent cidal activity was observed with a maximal kill of over 2 log.sub.10 CFU/kidney. Average 24 h AUC over 7 days was used to model AUC/MIC data and fit the treatment response data well with R.sup.2 0.70 for C. albicans and R.sup.2 0.86 for C. glabrata. The static dose (SD) and 1-log kill dose and associated AUC/MIC values are shown in Table 12.

(107) TABLE-US-00012 TABLE 12 Stasis 1 log kill Static Dose Ave 24 h 1 log kill dose Ave 24 h Strain MIC (mg/L) (mg/kg) AUC/MIC (mg/kg) AUC/MIC C. albicans K-1 0.008 2.52 3426 5.26 6435 580 0.016 1.20 948 2.03 1429 98-17  0.06 1.34 274 2.73 490 98-210 0.016 1.06 868 2.28 1574 C. glabrata 10956 0.5 6.29 120 17.3 301 5592 0.06 0.03 21.7 0.51 114 35315 0.25 0.34 17.9 2.39 105

(108) Conclusions

(109) CD101 demonstrated in vivo potency in the neutropenic murine disseminated candidiasis model against select C. albicans and C. glabrata strains. Similar to studies with other echinocandins, AUC/MIC fit the exposure-response data well and C. glabrata targets were numerically lower than C. albicans. PK/PD targets identified in this study will be useful for clinical dosing regimen optimization of CD101 in the context of human pharmacokinetics and MIC distribution.

Other Embodiments

(110) 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.

(111) While the disclosure 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 disclosure following, in general, the principles of the disclosure and including such departures from the present disclosure that come within known or customary practice within the art to which the disclosure pertains and may be applied to the essential features hereinbefore set forth, and follows in the scope of the claims. Other embodiments are within the claims.